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Mutations of the EPHA2 Receptor Tyrosine Kinase Gene Cause Autosomal Dominant Congenital Cataract
  • ISSN号：1059-7794
  • 期刊名称：Human Mutation
  • 时间：0
  • 页码：E603-E610
  • 语言：英文
  • 相关项目：重要出生缺陷遗传致病基因的识别及功能研究
作者： Zhang, Jinsong|Bhattacharya, Shomi S.|Moore, Anthony T.|Hua, Rui|Craig, Jamie E.|Luo, Yang|Zhang, Xue|Burdon, Kathryn P.|Zhang, Tianxiao|Mackey, David A.|Zhao, Xiuli|Shang, Dandan|Xiao, Wei|
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重要出生缺陷遗传致病基因的识别及功能研究
期刊论文 7
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