Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus-Reference-Cited by-同舟云学术

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Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus

Published:1995-07-01 Issue:7 Volume:4 Page:1119-1126
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Kolluri R.,Shehabeldin A.,Peacocke M.,Lamhonwah A.-M.,Teichert-Kuliszewska K.,Weissman S. M.,Siminovitch K. A.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/4/7/1119/2584717/4-7-1119.pdf

Cited by 96 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. Spectrum of WAS gene mutations in Vietnamese patients with Wiskott–Aldrich syndrome;Pediatrics International;2024-01

2. Understanding immunoactinopathies: A decade of research on WAS gene defects;Pediatric Allergy and Immunology;2023-04

3. Corrigendum to “WASP Family Proteins: Molecular Mechanisms and Implications in Human Disease” [Eur. J. Cell Biol. Vol. 101, Issue 3, (2022) 151244];European Journal of Cell Biology;2023-03

4. Not too little, not too much: the impact of mutation types in Wiskott-Aldrich syndrome and RAC2 patients;Clinical and Experimental Immunology;2023-01-06

5. Inadequate Activation of γδT- and B-cells in Patient with Wiskott-Aldrich Syndrome (WAS) Portrayed by TRG and IGH Repertoire Analyses;Journal of Clinical Immunology;2022-08-31

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