Chinese family with atypical granular corneal dystrophy type I caused by the typical R555W mutation in TGFBI

<b>AIM:</b> To investigate the clinical features and genetic defects in four generations of a Chinese family affected with atypical granular corneal dystrophy type I (GCD type I).<b>METHODS:</b> Family history and clinical data were recorded. Genomic DNA samples were obtained...

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Bibliographic Details
Main Authors: Su-Juan Zhao, Ya-Nan Zhu, Xing-Chao Shentu, Qi Miao
Format: Article
Language:English
Published: Press of International Journal of Ophthalmology (IJO PRESS) 2013-08-01
Series:International Journal of Ophthalmology
Subjects:
Online Access:http://www.ijo.cn/en_publish/2013/4/20130409.pdf

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