A Unique Clinical Presentation of X-Linked Lymphoproliferative Syndrome With a Novel Mutation in SH2D1A and Review of the Literature-Reference-Cited by-同舟云学术

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A Unique Clinical Presentation of X-Linked Lymphoproliferative Syndrome With a Novel Mutation in SH2D1A and Review of the Literature

Published:2011-01 Issue:1 Volume:33 Page:e39-e42
ISSN:1077-4114
Container-title:Journal of Pediatric Hematology/Oncology
language:en
Short-container-title:

Author:

Eckrich Michael J.,Yang Elizabeth,Domm Jennifer,Ho Richard,Calder Cassie,Manes Becky,Bleesing Jack,Frangoul Haydar

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Reference1 articles.

1. Immune deficiency in the X-linked lymphoproliferative syndrome. I.;Harada;Epstein-Barr virus-specific defects J Immunol,1982

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Exon skipping caused by a complex structural variation in SH2D1A resulted in X‐linked lymphoproliferative syndrome type 1;Molecular Genetics & Genomic Medicine;2022-01-29

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