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A D1424N mutation in the MYH9 gene results in macrothrombocytopenia and granulocytic inclusion bodies in a Chinese inherited macrothrombocytopenia pedigree.

Xin GuoXiaoqiang LianWenchao ZhangJihong Hao
Published in: Clinical chemistry and laboratory medicine (2019)
Keyphrases
  • hypertrophic cardiomyopathy
  • copy number
  • genome wide
  • genome wide identification
  • gene expression
  • left ventricular
  • transcription factor
  • genome wide analysis