中文

A de novo mutation of SMYD1 (p.F272L) is responsible for hypertrophic cardiomyopathy in a Chinese patient

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  • Release time:2018-09-27

  • Impact Factor:3.595

  • Journal:Clin Chem Lab Med

  • Co-author:Xiang R, Xia K, Jin J Y, Chen Y Q, Huang H, Ding D B, Fan L L

  • Indexed by:Unit Twenty Basic Research

  • Discipline:生物学

  • Document Type:J

  • Volume:57

  • Issue:4

  • Page Number:532-539

  • Translation or Not:no

  • Date of Publication:2019-04-01

  • Included Journals:SCI

  • Links to published journals:https://www.degruyter.com/view/j/cclm.2019.57.issue-4/cclm-2018-0578/cclm-2018-0578.xml


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