Clinical and molecular characteristics of Chinese patients with X-linked lymphoproliferative syndrome type 1-Reference-Cited by-同舟云学术

Clinical and molecular characteristics of Chinese patients with X-linked lymphoproliferative syndrome type 1

Published:2014-07-15 Issue:11 Volume:61 Page:2043-2047
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

An Yun-Fei¹²,Luo Xiao-Bo¹,Yang Xi¹,Wang Jing¹,Li Li¹,Zhao Xiao-Dong¹²

Affiliation:

1. Ministry of Education Key Laboratory of Child Development and Disorders; Children's Hospital of Chongqing Medical University; Chongqing China

2. Division of Immunology; Children's Hospital of Chongqing Medical University; Chongqing China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pbc.25126/fullpdf

Reference21 articles.

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2. X-linked lymphoproliferative disease: Twenty-five years after the discovery;Seemayer;Pediatr Res,1995

3. XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome;Rigaud;Nature,2006

4. X-linked lymphoproliferative syndromes: Brothers or distant cousins;Filipovich;Blood,2010

5. The SAP and SLAM families in immune responses and X-linked lymphoproliferative disease;Engel;Nat Rev Immunol,2003

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3. X-linked lymphoproliferative syndrome in mainland China: review of clinical, genetic, and immunological characteristic;European Journal of Pediatrics;2019-11-21

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