Molecular and structural characterization of five novel mutations in the Bruton's tyrosine kinase gene from patients with X-linked agammaglobulinemia.

Samankaltaisia teoksia

• X-Linked Agammaglobulinemia Case with TH Domain Missense Mutation in Bruton Tyrosine Kinase
  Tekijä: Agrebi, Nourhen, et al.
  Julkaistu: (2021)
• Novel deletion mutation in Bruton’s tyrosine kinase results in X-linked agammaglobulinemia: A case report
  Tekijä: Hu, Xiao-Mei, et al.
  Julkaistu: (2020)
• X-chromosome inactivation and mutation pattern in the Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinemia. Italian XLA Collaborative Group.
  Tekijä: Moschese, V., et al.
  Julkaistu: (2000)
• Genomic organization and structure of Bruton agammaglobulinemia tyrosine kinase: localization of mutations associated with varied clinical presentations and course in X chromosome-linked agammaglobulinemia.
  Tekijä: Ohta, Y, et al.
  Julkaistu: (1994)
• A novel Bruton’s tyrosine kinase gene (BTK) missense mutation in a Chinese family with X-linked agammaglobulinemia
  Tekijä: Zheng, Bixia, et al.
  Julkaistu: (2014)