A recurrent mutation in CRYGD is associated with autosomal dominant congenital coralliform cataract in two unrelated Chinese families

PURPOSE: Congenital cataract is a clinically and genetically heterogeneous lens disorder. The purpose of this study was to identify the mutation responsible for autosomal dominant congenital coralliform cataracts in two Chinese families and to investigate the relationship between virulence genes and...

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Detalles Bibliográficos
Autores principales: Yang, Guoxing, Xiong, Chunlei, Li, Shanlan, Wang, Yuanyuan, Zhao, Jialiang
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3086606/
https://www.ncbi.nlm.nih.gov/pubmed/21552497

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3086606/
https://www.ncbi.nlm.nih.gov/pubmed/21552497

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