Mutations of theEPHA2receptor tyrosine kinase gene cause autosomal dominant congenital cataract-Reference-Cited by-同舟云学术

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Mutations of theEPHA2receptor tyrosine kinase gene cause autosomal dominant congenital cataract

Published:2009-05 Issue:5 Volume:30 Page:E603-E611
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Zhang Tianxiao,Hua Rui,Xiao Wei,Burdon Kathryn P.,Bhattacharya Shomi S.,Craig Jamie E.,Shang Dandan,Zhao Xiuli,Mackey David A.,Moore Anthony T.,Luo Yang,Zhang Jinsong,Zhang Xue

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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