A novel insertional mutation in the connexin 46 (gap junction alpha 3) gene associated with autosomal dominant congenital cataract in a Chinese family

A novel insertional mutation in the connexin 46 (gap junction alpha 3) gene associated with autosomal dominant congenital cataract in a Chinese family

Bibliographic Details
Main Authors: Zhou, Dingan, Ji, Hongyun, Wei, Zhiyun, Guo, Luo, Li, Yanpeng, Wang, Teng, Zhu, Yu, Dong, Xingran, Wang, Yang, He, Lin, Xing, Qinghe, Zhang, Lirong
Format: Online
Language:English
Published: Molecular Vision 2013
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3626289/

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3626289/

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