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A germline or de novo mutation in two families with Gaucher disease: implications for recessive disorders

A germline or de novo mutation in two families with Gaucher disease: implications for recessive disorders

Saranjam, Hamid; Chopra, Sameer S; Levy, Harvey; Stubblefield, Barbara K; Maniwang, Emerson; Cohen, Ian J; Baris, Hagit; Sidransky, Ellen; Tayebi, Nahid
  • 期刊名称European Journal of Human Genetics
  • 作者Saranjam, Hamid; Chopra, Sameer S; Levy, Harvey; Stubblefield, Barbara K; Maniwang, Emerson; Cohen, Ian J; Baris, Hagit; Sidransky, Ellen; Tayebi, Nahid
  • 卷第21卷
  • 期第1期
  • 印刷ISSN1018-4813
  • 电子ISSN1476-5438
  • 文件大小344.03KB
  • 发表时间2013-1
  • DOI10.1038/ejhg.2012.105
  • 页码115-117
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