Associated Papers
Clinical characteristics and genetic profiles of 174 patients with X-linked agammaglobulinemia: Report from Shanghai, China (2000-2015).
Chen XF et al.
Medicine, 2016
Characterization of all possible single-nucleotide change caused amino acid substitutions in the kinase domain of Bruton tyrosine kinase.
Väliaho J et al.
Human Mutation, 2015
Clinical characteristics and molecular analysis of 21 Chinese children with congenital agammaglobulinemia.
Zhang ZY et al.
Scandinavian Journal of Immunology, 2010
[Analysis of mutation in heavy chain-micro (microHC) gene in a Chinese patient with congenital agammaglobulinemia].
Zhang ZY et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2010
[Genetic diagnosis of patients with primary agammaglobulinemia treated at third level peruvian centers].
Matos-Benavides E et al.
Revista Peruana De Medicina Experimental Y Salud Publica, 0
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