Novel mutations in FZD4 and phenotype–genotype correlation in Chinese patients with familial exudative vitreoretinopathy

PURPOSE: To identify novel mutations in the frizzled 4 (FZD4) gene in patients with familial exudative vitreoretinopathy (FEVR) in southern China and to delineate the mutation-associated clinical manifestations. METHODS: Clinical data and genomic DNA were collected from 100 probands and their family...

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Detalles Bibliográficos
Autores principales: Tang, Miao, Ding, Xiaoyan, Li, Jiaqing, Hu, Andina, Yuan, Miner, Yang, Yu, Zhan, Zongyi, Li, Zijing, Lu, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968609/
https://www.ncbi.nlm.nih.gov/pubmed/27555740

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968609/
https://www.ncbi.nlm.nih.gov/pubmed/27555740

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