Molecular Etiology of Isolated Congenital Cataract Using Next-Generation Sequencing: Single Center Exome Sequencing Data from Turkey

Congenital cataract, which refers to lenticular opacity diagnosed at birth or more commonly during the first year of life, is one of the leading causes of childhood blindness. Molecular understanding of the disease pathogenesis has evolved thanks to many studies based on modern technologies. In this...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Mol Syndromol
Prif Awduron: Taylan Sekeroglu, Hande, Karaosmanoglu, Beren, Taskiran, Ekim Z., Simsek Kiper, Pelin O., Alikasifoglu, Mehmet, Boduroglu, Koray, Coskun, Turgay, Utine, Gulen Eda
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: S. Karger AG 2020
Pynciau:
Original Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7802443/
https://ncbi.nlm.nih.gov/pubmed/33510601
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000510481
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