Idézéskapcsolat

Pechhacker Monika K. et al. CRB1-related retinopathy overlapping the ocular phenotype of S-adenosylhomocysteine hydrolase deficiency. (2020) OPHTHALMIC GENETICS 1381-6810

Közlemény:
Vamos R et al. Leber congenital amaurosis: first genotyped Hungarian patients and report of 2 novel mutations in the CRB1 and CEP290 genes.. (2016) EUROPEAN JOURNAL OF OPHTHALMOLOGY 1120-6721 1724-6016 26 1 78-84
Idéző közlemény:
Pechhacker Monika K. et al. CRB1-related retinopathy overlapping the ocular phenotype of S-adenosylhomocysteine hydrolase deficiency. (2020) OPHTHALMIC GENETICS 1381-6810
Független: Igen
2021-05-06 12:25