A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency-Reference-Cited by-同舟云学术

A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency

Published:2019-04 Issue:4 Volume:143 Page:1649-1653.e3
ISSN:0091-6749
Container-title:Journal of Allergy and Clinical Immunology
language:en
Short-container-title:Journal of Allergy and Clinical Immunology

Author:

Lougaris Vassilios,Chou Janet,Beano Abdallah,Wallace Jacqueline G.,Baronio Manuela,Gazzurelli Luisa,Lorenzini Tiziana,Moratto Daniele,Tabellini Giovanna,Parolini Silvia,Seleman Michael,Stafstrom Kelsey,Xu Haiming,Harris Chad,Geha Raif S.,Plebani Alessandro

Funder

European Community's Seventh Framework Programme

EURO-PADnet HEALTH

Italian Ministerial Grant

Fondazione C. Golgi

Jeffrey Modell Foundation

Perkin Fund

National Institutes of Health

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference14 articles.

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3. Dominant negative mutation of the hematopoietic-specific Rho GTPase, Rac2, is associated with a human phagocyte immunodeficiency;Williams;Blood,2000

4. RAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency;Alkhairy;J Allergy Clin Immunol,2015

5. Human phagocyte defect caused by a Rac2 mutation detected by means of neonatal screening for T-cell lymphopenia;Accetta;J Allergy Clin Immunol,2011

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