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Inherited KIF21A and PAX6 gene mutations in a boy with congenital fibrosis of extraocular muscles an
  • ISSN号：1471-2350
  • 期刊名称：BMC Medical Genetics
  • 时间：2013.6.21
  • 页码：63-
  • 相关项目：BRR2蛋白突变导致视网膜色素变性发病机制的研究
作者： Han Ruifang|Hao Peng|Wang Liming|Li Ningdong|
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BRR2蛋白突变导致视网膜色素变性发病机制的研究
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