Novel mutations in CRYGC are associated with congenital cataracts in Chinese families

Novel mutations in CRYGC are associated with congenital cataracts in Chinese families

Abstract Congenital cataract (CC), responsible for about one-third of blindness in infants, is a major cause of vision loss in children worldwide. 10–25% of CC cases are attributed to genetic causes and CC is a clinically and genetically highly heterogeneous lens disorder in children. Autosomal domi...

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Bibliographic Details
Main Authors:	Zilin Zhong, Zehua Wu, Liyun Han, Jianjun Chen
Format:	Article
Language:	English
Published:	Nature Publishing Group 2017-03-01
Series:	Scientific Reports
Online Access:	https://doi.org/10.1038/s41598-017-00318-1

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