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