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...

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Detaylı Bibliyografya
Yayımlandı:Mol Syndromol
Asıl Yazarlar: Taylan Sekeroglu, Hande, Karaosmanoglu, Beren, Taskiran, Ekim Z., Simsek Kiper, Pelin O., Alikasifoglu, Mehmet, Boduroglu, Koray, Coskun, Turgay, Utine, Gulen Eda
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: S. Karger AG 2020
Konular:
Original Article
Online Erişim: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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