טוען...

A novel mutation in CRYAB associated with autosomal dominant congenital nuclear cataract in a Chinese family

PURPOSE: To identify the genetic defects associated with autosomal dominant congenital nuclear cataract in a Chinese family. METHODS: Clinical data were collected, and the phenotypes of the affected members in this family were recorded by slit-lamp photography. Genomic DNA was isolated from peripher...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
Main Authors: Chen, Qiang, Ma, Junjie, Yan, Ming, Mothobi, Maneo Emily, Liu, Yuanyuan, Zheng, Fang
פורמט: Artigo
שפה:Inglês
יצא לאור: Molecular Vision 2009
נושאים:
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC2709425/
https://ncbi.nlm.nih.gov/pubmed/19597569
תגים: הוספת תג
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