Characterization of SH2D1A Missense Mutations Identified in X-linked Lymphoproliferative Disease Patients-Reference-Cited by-同舟云学术

Characterization of SH2D1A Missense Mutations Identified in X-linked Lymphoproliferative Disease Patients

Published:2001-09 Issue:39 Volume:276 Page:36809-36816
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Morra Massimo,Simarro-Grande Maria,Martin Margarita,Chen Alice Siau-In,Lanyi Arpad,Silander Olin,Calpe Silvia,Davis Jack,Pawson Tony,Eck Michael J.,Sumegi Janos,Engel Pablo,Li Shun-Cheng,Terhorst Cox

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference40 articles.

1. X-LINKED RECESSIVE PROGRESSIVE COMBINED VARIABLE IMMUNODEFICIENCY (DUNCAN'S DISEASE)

2. X-Linked Lymphoproliferative Disease: Twenty-Five Years after the Discovery

3. The abnormal gene in X-linked lymphoproliferative syndrome

4. The gene defective in X-linked lymphoproliferative disease controls T cell dependent immune surveillance against Epstein–Barr virus

5. X-Linked Lymphoproliferative Disease: A Progressive Immunodeficiency

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