{ "labelLang" : "eng", "responseDate" : "2024-03-28 16:32", "content" : { "otype" : "Citation", "mtid" : 22350239, "status" : "APPROVED", "published" : true, "comment" : "Molecular Sequence Numbers: GENBANK: L06133, Z94801;\nChemicals/CAS: adenosine triphosphatase, 37289-25-1, 9000-83-3; amino acid, 65072-01-7; copper, 15158-11-9, 7440-50-8; Adenosine Triphosphatases, EC 3.6.1.-; ATP7A protein, human, EC 3.6.3.4; Cation Transport Proteins; DNA Primers; Recombinant Fusion Proteins", "unhandledTickets" : 0, "oldTimestamp" : "2018-10-01T21:33:57.000+0000", "deleted" : false, "oldId" : 12350239, "lastRefresh" : "2023-09-20T00:11:53.431+0000", "lastModified" : "2018-10-01T21:33:57.000+0000", "created" : "2012-06-05T21:09:03.000+0000", "publication" : { "otype" : "JournalArticle", "mtid" : 1808465, "link" : "/api/publication/1808465", "label" : "Bachrati CZ et al. Carrier detection by microsatellite analysis of Duchenne/Becker muscular dystrophy in Hungarian families. (1998) ANNALS OF HUMAN GENETICS 0003-4800 1469-1809 62 6 511-520", "core" : true, "citation" : false, "publicationPending" : false, "type" : { "otype" : "PublicationType", "mtid" : 24, "link" : "/api/publicationtype/24", "label" : "Journal Article", "code" : 24, "otypeName" : "JournalArticle", "listPosition" : 1, "published" : true, "oldId" : 24, "snippet" : true }, "subType" : { "otype" : "SubType", "mtid" : 10000059, "link" : "/api/subtype/10000059", "label" : "Article (Journal Article)", "name" : "Szakcikk", "nameEng" : "Article", "docType" : { "otype" : "PublicationType", "mtid" : 24, "link" : "/api/publicationtype/24", "label" : "Journal Article", "code" : 24, "otypeName" : "JournalArticle", "listPosition" : 1, "published" : true, "oldId" : 24, "snippet" : true }, "listPosition" : 101, "published" : true, "oldId" : 10000059, "snippet" : true }, "category" : { "otype" : "Category", "mtid" : 1, "link" : "/api/category/1", "label" : "Scientific", "published" : true, "oldId" : 1, "snippet" : true }, "languages" : [ { "otype" : "Language", "mtid" : 10002, "link" : "/api/language/10002", "label" : "English", "name" : "Angol", "nameEng" : "English", "published" : true, "oldId" : 2, "snippet" : true } ], "title" : "Carrier detection by microsatellite analysis of Duchenne/Becker muscular dystrophy in Hungarian families", "identifiers" : [ { "otype" : "PublicationIdentifier", "mtid" : 461499, "link" : "/api/publicationidentifier/461499", "label" : "DOI: 10.1017/S0003480099007216", "source" : { "otype" : "PlainSource", "mtid" : 6, "link" : "/api/publicationsource/6", "label" : "DOI", "type" : { "otype" : "PublicationSourceType", "mtid" : 10001, "link" : "/api/publicationsourcetype/10001", "label" : "DOI", "mayHaveOa" : true, "published" : true, "snippet" : true }, "name" : "DOI", "nameEng" : "DOI", "linkPattern" : "https://doi.org/@@@", "publiclyVisible" : true, "published" : true, "oldId" : 6, "snippet" : true }, "oaFree" : false, "validState" : "IDENTICAL", "idValue" : "10.1017/S0003480099007216", "realUrl" : "https://doi.org/10.1017/S0003480099007216", "published" : false, "oldId" : 274195, "snippet" : true }, { "otype" : "PublicationIdentifier", "mtid" : 461500, "link" : "/api/publicationidentifier/461500", "label" : "DOI: 10.1046/j.1469-1809.1998.6260511.x", "source" : { "otype" : "PlainSource", "mtid" : 6, "link" : "/api/publicationsource/6", "label" : "DOI", "type" : { "otype" : "PublicationSourceType", "mtid" : 10001, "link" : "/api/publicationsourcetype/10001", "label" : "DOI", "mayHaveOa" : true, "published" : true, "snippet" : true }, "name" : "DOI", "nameEng" : "DOI", "linkPattern" : "https://doi.org/@@@", "publiclyVisible" : true, "published" : true, "oldId" : 6, "snippet" : true }, "oaFree" : false, "validState" : "IDENTICAL", "idValue" : "10.1046/j.1469-1809.1998.6260511.x", "realUrl" : "https://doi.org/10.1046/j.1469-1809.1998.6260511.x", "published" : false, "oldId" : 1136435, "snippet" : true }, { "otype" : "PublicationIdentifier", "mtid" : 461497, "link" : "/api/publicationidentifier/461497", "label" : "WoS: 000080555000005", "source" : { "otype" : "PlainSource", "mtid" : 1, "link" : "/api/publicationsource/1", "label" : "WoS", "type" : { "otype" : "PublicationSourceType", "mtid" : 10003, "link" : "/api/publicationsourcetype/10003", "label" : "Indexelő adatbázis", "mayHaveOa" : false, "published" : true, "snippet" : true }, "name" : "WoS", "nameEng" : "WoS", "linkPattern" : "https://www.webofscience.com/wos/woscc/full-record/@@@", "publiclyVisible" : true, "published" : true, "oldId" : 1, "snippet" : true }, "oaFree" : false, "validState" : "IDENTICAL", "idValue" : "000080555000005", "realUrl" : "https://www.webofscience.com/wos/woscc/full-record/000080555000005", "published" : false, "oldId" : 1049867, "snippet" : true }, { "otype" : "PublicationIdentifier", "mtid" : 461498, "link" : "/api/publicationidentifier/461498", "label" : "Scopus: 0032419344", "source" : { "otype" : "PlainSource", "mtid" : 3, "link" : "/api/publicationsource/3", "label" : "Scopus", "type" : { "otype" : "PublicationSourceType", "mtid" : 10003, "link" : "/api/publicationsourcetype/10003", "label" : "Indexelő adatbázis", "mayHaveOa" : false, "published" : true, "snippet" : true }, "name" : "Scopus", "linkPattern" : "http://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-@@@", "publiclyVisible" : true, "published" : true, "oldId" : 3, "snippet" : true }, "oaFree" : false, "validState" : "IDENTICAL", "idValue" : "0032419344", "realUrl" : "http://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-0032419344", "published" : false, "oldId" : 274196, "snippet" : true }, { "otype" : "PublicationIdentifier", "mtid" : 461501, "link" : "/api/publicationidentifier/461501", "label" : "PubMed: 10363129", "source" : { "otype" : "PlainSource", "mtid" : 17, "link" : "/api/publicationsource/17", "label" : "PubMed", "type" : { "otype" : "PublicationSourceType", "mtid" : 10003, "link" : "/api/publicationsourcetype/10003", "label" : "Indexelő adatbázis", "mayHaveOa" : false, "published" : true, "snippet" : true }, "name" : "PubMed", "nameEng" : "PubMed", "linkPattern" : "http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=@@@&dopt=Abstract", "publiclyVisible" : true, "published" : true, "oldId" : 17, "snippet" : true }, "oaFree" : false, "validState" : "IDENTICAL", "idValue" : "10363129", "realUrl" : "http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=10363129&dopt=Abstract", "published" : false, "oldId" : 274197, "snippet" : true }, { "otype" : "PublicationIdentifier", "mtid" : 461502, "link" : "/api/publicationidentifier/461502", "label" : "SZTE Publicatio: 10218", "source" : { "otype" : "SwordSource", "mtid" : 90, "link" : "/api/publicationsource/90", "label" : "SZTE Publicatio", "type" : { "otype" : "PublicationSourceType", "mtid" : 10007, "link" : "/api/publicationsourcetype/10007", "label" : "Repozitórium", "mayHaveOa" : true, "published" : true, "snippet" : true }, "name" : "SZTE Publicatio", "nameEng" : "SZTE Publicatio", "linkPattern" : "http://publicatio.bibl.u-szeged.hu/@@@", "publiclyVisible" : true, "published" : true, "oldId" : 90, "snippet" : true }, "oaType" : "GREEN", "oaFree" : false, "validState" : "IDENTICAL", "idValue" : "10218", "realUrl" : "http://publicatio.bibl.u-szeged.hu/10218", "published" : false, "oldId" : 1515518, "snippet" : true } ], "journal" : { "otype" : "Journal", "mtid" : 348, "link" : "/api/journal/348", "label" : "ANNALS OF HUMAN GENETICS 0003-4800 1469-1809", "pIssn" : "0003-4800", "eIssn" : "1469-1809", "reviewType" : "REVIEWED", "noIF" : false, "sciIndexed" : true, "scopusIndexed" : true, "lang" : "FOREIGN", "hungarian" : false, "published" : true, "oldId" : 348, "snippet" : true }, "volume" : "62", "issue" : "6", "publishedAt" : [ ], "pageLength" : 10, "publishedYear" : 1998, "foreignEdition" : true, "foreignLanguage" : true, "fullPublication" : true, "conferencePublication" : false, "nationalOrigin" : true, "oaLink" : "http://publicatio.bibl.u-szeged.hu/10218", "published" : true, "oldId" : 1808465, "snippet" : true }, "publicationMtid" : 1808465, "related" : { "otype" : "JournalArticle", "mtid" : 22350239, "link" : "/api/publication/22350239", "label" : "Poulsen L et al. X-linked recessive Menkes disease: Identification of partial gene deletions in affected males. (2002) CLINICAL GENETICS 0009-9163 1399-0004 62 6 449-457", "core" : false, "citation" : true, "publicationPending" : false, "type" : { "otype" : "PublicationType", "mtid" : 24, "link" : "/api/publicationtype/24", "label" : "Journal Article", "code" : 24, "otypeName" : "JournalArticle", "listPosition" : 1, "published" : true, "oldId" : 24, "snippet" : true }, "languages" : [ { "otype" : "Language", "mtid" : 10002, "link" : "/api/language/10002", "label" : "English", "name" : "Angol", "nameEng" : "English", "published" : true, "oldId" : 2, "snippet" : true } ], "title" : "X-linked recessive Menkes disease: Identification of partial gene deletions in affected males", "identifiers" : [ { "otype" : "PublicationIdentifier", "mtid" : 4919086, "link" : "/api/publicationidentifier/4919086", "label" : "DOI: 10.1034/j.1399-0004.2002.620605.x", "source" : { "otype" : "PlainSource", "mtid" : 6, "link" : "/api/publicationsource/6", "label" : "DOI", "type" : { "otype" : "PublicationSourceType", "mtid" : 10001, "link" : "/api/publicationsourcetype/10001", "label" : "DOI", "mayHaveOa" : true, "published" : true, "snippet" : true }, "name" : "DOI", "nameEng" : "DOI", "linkPattern" : "https://doi.org/@@@", "publiclyVisible" : true, "published" : true, "oldId" : 6, "snippet" : true }, "validState" : "NO", "idValue" : "10.1034/j.1399-0004.2002.620605.x", "realUrl" : "https://doi.org/10.1034/j.1399-0004.2002.620605.x", "published" : false, "oldId" : 2207732, "snippet" : true }, { "otype" : "PublicationIdentifier", "mtid" : 4919084, "link" : "/api/publicationidentifier/4919084", "label" : "WoS: 000179771800007", "source" : { "otype" : "PlainSource", "mtid" : 1, "link" : "/api/publicationsource/1", "label" : "WoS", "type" : { "otype" : "PublicationSourceType", "mtid" : 10003, "link" : "/api/publicationsourcetype/10003", "label" : "Indexelő adatbázis", "mayHaveOa" : false, "published" : true, "snippet" : true }, "name" : "WoS", "nameEng" : "WoS", "linkPattern" : "https://www.webofscience.com/wos/woscc/full-record/@@@", "publiclyVisible" : true, "published" : true, "oldId" : 1, "snippet" : true }, "validState" : "NO", "idValue" : "000179771800007", "realUrl" : "https://www.webofscience.com/wos/woscc/full-record/000179771800007", "published" : false, "oldId" : 4050009, "snippet" : true }, { "otype" : "PublicationIdentifier", "mtid" : 4919085, "link" : "/api/publicationidentifier/4919085", "label" : "Scopus: 0036953710", "source" : { "otype" : "PlainSource", "mtid" : 3, "link" : "/api/publicationsource/3", "label" : "Scopus", "type" : { "otype" : "PublicationSourceType", "mtid" : 10003, "link" : "/api/publicationsourcetype/10003", "label" : "Indexelő adatbázis", "mayHaveOa" : false, "published" : true, "snippet" : true }, "name" : "Scopus", "linkPattern" : "http://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-@@@", "publiclyVisible" : true, "published" : true, "oldId" : 3, "snippet" : true }, "validState" : "NO", "idValue" : "0036953710", "realUrl" : "http://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-0036953710", "published" : false, "oldId" : 2207733, "snippet" : true } ], "journal" : { "otype" : "Journal", "mtid" : 1052, "link" : "/api/journal/1052", "label" : "CLINICAL GENETICS 0009-9163 1399-0004", "pIssn" : "0009-9163", "eIssn" : "1399-0004", "reviewType" : "REVIEWED", "noIF" : false, "sciIndexed" : true, "scopusIndexed" : true, "lang" : "FOREIGN", "hungarian" : false, "published" : true, "oldId" : 1052, "snippet" : true }, "volume" : "62", "issue" : "6", "publishedAt" : [ ], "pageLength" : 9, "publishedYear" : 2002, "foreignEdition" : true, "foreignLanguage" : true, "fullPublication" : false, "published" : true, "oldId" : 12350239, "snippet" : true }, "relatedMtid" : 22350239, "source" : "Scopus-RIS", "externalCitation" : true, "externalCitationOK" : true, "mentionCount" : 1, "link" : "/api/citation/22350239", "label" : "Poulsen L et al. X-linked recessive Menkes disease: Identification of partial gene deletions in affected males. (2002) CLINICAL GENETICS 0009-9163 1399-0004 62 6 449-457", "template" : "