中文

Whole exome sequencing identifies a novel mutation (c.333 + 2T > C) of TNNI3K in a Chinese family with dilated cardiomyopathy and cardiac conduction disease

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  • Release time:2018-01-20

  • Impact Factor:2.984

  • Journal:Gene

  • Co-author:Xiang R, Zhao S P, Chen Y Q, Li J J, Jin J Y, Huang H, Fan L L

  • Indexed by:Unit Twenty Basic Research

  • Discipline:生物学

  • Document Type:J

  • Volume:648

  • Issue:2018

  • Page Number:63-67

  • Translation or Not:no

  • Date of Publication:2018-01-20

  • Included Journals:SCI

  • Links to published journals:https://www.sciencedirect.com/science/article/pii/S0378111918300696


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