Mutation screening of crystallin genes in Chinese families with congenital cataracts

PURPOSE: To identify mutations in crystallin genes in Chinese families with congenital cataracts. METHODS: Forty-two unrelated families with non-syndromic congenital cataracts were enrolled in this study. The coding exons and adjacent intronic regions of crystallin genes, including CRYAA, CRYAB, CRY...

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Detalles Bibliográficos
Autores principales: Zhuang, Jianfu, Cao, Zongfu, Zhu, Yihua, Liu, Lijuan, Tong, Yi, Chen, Xiaole, Wang, Yaduan, Lu, Cailing, Ma, Xu, Yang, Juhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707615/
https://www.ncbi.nlm.nih.gov/pubmed/31523120

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707615/
https://www.ncbi.nlm.nih.gov/pubmed/31523120

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