Identification of FZD4 and LRP5 mutations in 11 of 49 families with familial exudative vitreoretinopathy

PURPOSE: To identify mutations in FZD4 and LRP5 in 49 Chinese families with familial exudative vitreoretinopathy (FEVR) and to reveal the mutation spectrum and frequency of these genes in the Chinese population. METHODS: Clinical data and genomic DNA were collected for patients from 49 families with...

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Detalles Bibliográficos
Autores principales: Yang, Huiqin, Li, Shiqiang, Xiao, Xueshan, Wang, Panfeng, Guo, Xiangming, Zhang, Qingjiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472927/
https://www.ncbi.nlm.nih.gov/pubmed/23077402

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472927/
https://www.ncbi.nlm.nih.gov/pubmed/23077402

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