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Autosomal recessive hyper-IgE syndrome in two brothers of a Chinese family with a novel mutation in DOCK8 gene.

Shan WangW MouZ XuJ GuiL Ma
Published in: Journal of the European Academy of Dermatology and Venereology : JEADV (2018)
Keyphrases
  • copy number
  • genome wide
  • intellectual disability
  • case report
  • genome wide identification
  • muscular dystrophy
  • gene expression
  • transcription factor