Associated Papers
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
Mutation screening of the BTK gene in 56 families with X-linked agammaglobulinemia (XLA): 47 unique mutations without correlation to clinical course.
Holinski-Feder E et al.
Pediatrics, 1998
Select a paper to view details