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Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1
  • ISSN号：1090-0535
  • 期刊名称：Molecular Vision
  • 时间：2013.3.3
  • 页码：695-701
  • 相关项目：BCAS2功能与白内障致病机制
作者： Liu, Mugen|Li, Pengcheng|Liu, Ying|Li, Weirong|Wong, Fulton|Du, Rong|Wang, Lei|Li, Chang|Jiang, Fagang|
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BCAS2功能与白内障致病机制
期刊论文 7
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