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X-Linked Agammaglobulinemia Case with TH Domain Missense Mutation in Bruton Tyrosine Kinase.

Nourhen AgrebiGiusy GentilcoreJean-Charles GrivelGhroob AlkhayerJihad HassounAmel HassanMehdi AdeliBernice Lo
Published in: Journal of clinical immunology (2021)
Keyphrases
  • tyrosine kinase
  • epidermal growth factor receptor
  • intellectual disability
  • autism spectrum disorder