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Novel mutations associated with autosomal-dominant congenital cataract identified in Chinese families

As the leading cause of impaired vision, congenital cataracts, particularly autosomal dominant congenital cataract (ADCC), have been considered as a hereditary disease. The present study aimed to identify genetic defects in Chinese pedigrees with ADCC. A total of 6 Chinese families with ADCC were in...

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Detalhes bibliográficos
Publicado no:Exp Ther Med
Main Authors: Wang, Zhenyu, Huang, Chen, Sun, Yanxiu, Lv, Huibin, Zhang, Mingzhou, Li, Xuemin
Formato: Artigo
Idioma:Inglês
Publicado em: D.A. Spandidos 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6755416/
https://ncbi.nlm.nih.gov/pubmed/31555371
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2019.7865
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