A Novel Mutation in CRYGC Mutation Associated with Autosomal Dominant Congenital Cataracts and Microcornea

A Novel Mutation in CRYGC Mutation Associated with Autosomal Dominant Congenital Cataracts and Microcornea

Purpose: Crystallin protein mutations are associated with congenital cataract (CC), and several disease-causing mutations in the CRYGC gene have been identified. We present the location of a new mutation in CRYGC in members of a Chinese family who presented with CCs with or without microcornea. Desi...

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Bibliographic Details
Main Authors: Zhenbao Zhou, MD, Liying Zhao, MD, Yanqin Guo, MD, Jingyi Zhuang, MD, Nan Zhuo, MD, Han Chen, MD, Jieting Liu, MD, Libo Wang, MD
Format: Article
Language:English
Published: Elsevier 2022-03-01
Series:Ophthalmology Science
Subjects:
Congenital cataracts
CRYGC gene
Microcornea
Novel mutation
Online Access:http://www.sciencedirect.com/science/article/pii/S2666914521000944

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http://www.sciencedirect.com/science/article/pii/S2666914521000944

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