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