Clinical features and mutation analysis of X-linked agammaglobulinemia in 20 Chinese patients.

scientific article published on 18 January 2013

Clinical features and mutation analysis of X-linked agammaglobulinemia in 20 Chinese patients. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1007/S12519-013-0400-X
P698PubMed publication ID23335184

P2093author name stringLi-Ping Jiang
Xiao-Dong Zhao
Xue-Mei Tang
Mo Wang
Xian Qin
En-Mei Liu
P2860cites workGenetic defect in human X-linked agammaglobulinemia impedes a maturational evolution of pro-B cells into a later stage of pre-B cells in the B-cell differentiation pathwayQ28140283
Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies)Q28140427
AgammaglobulinemiaQ28244575
Clinical characteristics and molecular analysis of 21 Chinese children with congenital agammaglobulinemiaQ30155973
Mutation of the BTK gene and clinical feature of X-linked agammaglobulinemia in mainland ChinaQ30157453
Identification of novel Bruton's tyrosine kinase mutations in 10 unrelated subjects with X linked agammaglobulinaemiaQ33678961
The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinasesQ34355151
Mutations in btk in patients with presumed X-linked agammaglobulinemiaQ34385386
Bruton's tyrosine kinase: cell biology, sequence conservation, mutation spectrum, siRNA modifications, and expression profiling.Q34386319
The clinical spectrum of Bruton's agammaglobulinemiaQ34561843
X-linked immunodeficienciesQ35850633
Bruton's tyrosine kinase is a key regulator in B-cell developmentQ40694860
X-linked agammaglobulinemia and other immunoglobulin deficienciesQ40694868
[Gene diagnosis of X-linked agammaglobulinemia].Q55041072
Mutation screening of the BTK gene in 56 families with X-linked agammaglobulinemia (XLA): 47 unique mutations without correlation to clinical courseQ58482629
X-linked immune deficiency (xid) of CBA/N miceQ68798401
DNA-based mutation analysis of Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinaemiaQ72144580
Clinical and mutational characteristics of X-linked agammaglobulinemia and its carrier identified by flow cytometric assessment combined with genetic analysisQ77347952
Clinical findings leading to the diagnosis of X-linked agammaglobulinemiaQ78367574
Clinical characteristics and genotype-phenotype correlation in 62 patients with X-linked agammaglobulinemiaQ84880299
P433issue3
P304page(s)273-277
P577publication date2013-01-18
P1433published inWorld Journal of PediatricsQ15763275
P1476titleClinical features and mutation analysis of X-linked agammaglobulinemia in 20 Chinese patients.
P478volume9

Reverse relations

cites work (P2860)
Q33602552Clinical targeting of mutated and wild-type protein tyrosine kinases in cancer
Q35033817Splice-correction strategies for treatment of X-linked agammaglobulinemia.

Search more.