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Autosomal recessive hyper-IgE syndrome in two brothers of a Chinese family with a novel mutation in DOCK8 gene.
Shan Wang
W Mou
Z Xu
J Gui
L Ma
Published in:
Journal of the European Academy of Dermatology and Venereology : JEADV (2018)
Keyphrases
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copy number
genome wide
intellectual disability
case report
genome wide identification
muscular dystrophy
gene expression
transcription factor