Clinical and mutational features of Vietnamese children with X-linked agammaglobulinemia-Reference-Cited by-同舟云学术

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Clinical and mutational features of Vietnamese children with X-linked agammaglobulinemia

Published:2014-05-28 Issue:1 Volume:14 Page:
ISSN:1471-2431
Container-title:BMC Pediatrics
language:en
Short-container-title:BMC Pediatr

Author:

Vu Quang Van,Wada Taizo,Le Huong Thi Minh,Le Hai Thanh,Van Nguyen Anh Thi,Osamu Ohara,Yachie Akihiro,Nguyen Sang Ngoc

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1186/1471-2431-14-129.pdf

Reference27 articles.

1. Bruton OC: Agammaglobulinemia. Pediatrics. 1952, 9: 722-728.

2. Velickovic M, Prasad ML, Weston SA, Benson EM: Identification of the bruton tyrosine kinase (BTK) gene mutations in 20 Australian families with X-linked agammaglobulinemia (XLA). Hum Mutat. 2004, 23: 398-399.

3. Kristufek D, Aspalter RM, Eibl MM, Wolf HM: Characterization of novel Bruton’s tyrosine kinase gene mutations in central European patients with agammaglobulinemia. Mol Immunol. 2007, 44: 1639-1643. 10.1016/j.molimm.2006.08.003.

4. Fiorini M, Franceschini R, Soresina A, Schumacher R-F, Ugazio AG, Rossi P, Plebani A, Notarangelo LD: BTK: 22 novel and 25 recurrent mutations in European patients with X-linked agammaglobulinemia. Hum Mutat. 2004, 23: 286-

5. Zhang Z-Y, Zhao X-D, Jiang L-P, Liu E-M, Wang M, Yu J, Liu P, Yang X-Q: Clinical characteristics and molecular analysis of 21 Chinese children with congenital agammaglobulinemia. Scand J Immunol. 2010, 72: 454-459. 10.1111/j.1365-3083.2010.02457.x.

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