Novel mutations in HSF4 cause congenital cataracts in Chinese families

BACKGROUND: Congenital cataract, a kind of cataract presenting at birth or during early childhood, is a leading cause of childhood blindness. To date, more than 30 genes on different chromosomes are known to cause this disorder. This study aimed to identify the HSF4 mutations in a cohort from Chines...

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Detalles Bibliográficos
Autores principales: Cao, Zongfu, Zhu, Yihua, Liu, Lijuan, Wu, Shuangqing, Liu, Bing, Zhuang, Jianfu, Tong, Yi, Chen, Xiaole, Xie, Yongqing, Nie, Kaimei, Lu, Cailing, Ma, Xu, Yang, Juhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109319/
https://www.ncbi.nlm.nih.gov/pubmed/30143024
http://dx.doi.org/10.1186/s12881-018-0636-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109319/
https://www.ncbi.nlm.nih.gov/pubmed/30143024
http://dx.doi.org/10.1186/s12881-018-0636-3

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