Mutational screening of six genes in Chinese patients with congenital cataract and microcornea

PURPOSE: To identify mutations in 6 genes of 9 Chinese families with congenital cataract and microcornea. METHODS: Nine unrelated families with congenital cataract and microcornea were collected. Cycle sequencing was used to detect variants in the coding and adjacent regions of the crystallin alpha...

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Detalles Bibliográficos
Autores principales: Sun, Wenmin, Xiao, Xueshan, Li, Shiqiang, Guo, Xiangming, Zhang, Qingjiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3115747/
https://www.ncbi.nlm.nih.gov/pubmed/21686328

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3115747/
https://www.ncbi.nlm.nih.gov/pubmed/21686328

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