Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract

Tianxiao Zhang; Rui Hau; Wei Xiao; Kathryn Burdon; Shomi Bhattacharya; Jamie Craig; Dandan Shang; Xiuli Zhao; David Mackey; Anthony Moore; Yang Luo; Jinsong Zhang; Xue Zhang

Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract

Tianxiao Zhang, Rui Hau, Wei Xiao, Kathryn Burdon, Shomi Bhattacharya, Jamie Craig, Dandan Shang, Xiuli Zhao, David Mackey, Anthony Moore, Yang Luo, Jinsong Zhang, Xue Zhang

Research output: Contribution to journal › Article › peer-review

87 Citations (Scopus)

Original language	English
Pages (from-to)	E603-E611
Number of pages	9
Journal	Human Mutation
Volume	30
Issue number	5
Publication status	Published - 2009

Cite this

@article{7c532dee1b564a78ba8f85e26193c259,

title = "Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract",

author = "Tianxiao Zhang and Rui Hau and Wei Xiao and Kathryn Burdon and Shomi Bhattacharya and Jamie Craig and Dandan Shang and Xiuli Zhao and David Mackey and Anthony Moore and Yang Luo and Jinsong Zhang and Xue Zhang",

year = "2009",

language = "English",

volume = "30",

pages = "E603--E611",

journal = "Human Mutation",

issn = "1059-7794",

publisher = "Wiley-Liss Inc.",

number = "5",

}

TY - JOUR

T1 - Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract

AU - Zhang, Tianxiao

AU - Hau, Rui

AU - Xiao, Wei

AU - Burdon, Kathryn

AU - Bhattacharya, Shomi

AU - Craig, Jamie

AU - Shang, Dandan

AU - Zhao, Xiuli

AU - Mackey, David

AU - Moore, Anthony

AU - Luo, Yang

AU - Zhang, Jinsong

AU - Zhang, Xue

PY - 2009

Y1 - 2009

M3 - Article

VL - 30

SP - E603-E611

JO - Human Mutation

JF - Human Mutation

SN - 1059-7794

IS - 5

ER -