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MSTO1 is a cytoplasmic pro-mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans.
Gal, Aniko [Gál, Anikó (Molekuláris bioló...), author] Genomic Medicine and the Institute of Rare Dise... (SU / FM / I)
;
Balicza, Peter [Balicza, Péter (neurogenetika), author] Genomic Medicine and the Institute of Rare Dise... (SU / FM / I)
;
Weaver, David
;
Naghdi, Shamim
;
Joseph, Suresh K
;
Várnai, Péter [Várnai, Péter (Sejtélettan), author] Department of Physiology (SU / FM / I)
;
Gyuris, Tibor [Gyuris, Tibor (genomika), author]
;
Horváth, Attila
;
Nagy, Laszlo
;
Seifert, Erin L
;
Molnar, Maria Judit [Molnár, Mária Judit (Neurológia), author] Genomic Medicine and the Institute of Rare Dise... (SU / FM / I)
;
Hajnóczky, György ✉ [Hajnóczky, György (Orvosi élettan, e...), author]
English Comment, Correction (Journal Article) Scientific
Published:
EMBO MOLECULAR MEDICINE 1757-4676 1757-4684
15
Paper: e17911
2023
Identifiers
MTMT: 34066940
DOI:
10.15252/emmm.202317911
WoS:
001026881400001
Scopus:
85164522407
PubMed:
37431817
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2025-04-16 13:01
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