Whole-exome sequencing identifies tetratricopeptide repeat domain 7A ( TTC7A ) mutations for combined immunodeficiency with intestinal atresias-Reference-Cited by-同舟云学术

Whole-exome sequencing identifies tetratricopeptide repeat domain 7A ( TTC7A ) mutations for combined immunodeficiency with intestinal atresias

Published:2013-09 Issue:3 Volume:132 Page:656-664.e17
ISSN:0091-6749
Container-title:Journal of Allergy and Clinical Immunology
language:en
Short-container-title:Journal of Allergy and Clinical Immunology

Author:

Chen Rui,Giliani Silvia,Lanzi Gaetana,Mias George I.,Lonardi Silvia,Dobbs Kerry,Manis John,Im Hogune,Gallagher Jennifer E.,Phanstiel Douglas H.,Euskirchen Ghia,Lacroute Philippe,Bettinger Keith,Moratto Daniele,Weinacht Katja,Montin Davide,Gallo Eleonora,Mangili Giovanna,Porta Fulvio,Notarangelo Lucia D.,Pedretti Stefania,Al-Herz Waleed,Alfahdli Wasmi,Comeau Anne Marie,Traister Russell S.,Pai Sung-Yun,Carella Graziella,Facchetti Fabio,Nadeau Kari C.,Snyder Michael,Notarangelo Luigi D.

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

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5. Hereditary multiple intestinal atresia (HMIA) with severe combined immunodeficiency (SCID): a case report of two siblings and review of the literature on MIA, HMIA and HMIA with immunodeficiency over the last 50 years;Ali;BMJ Case Rep,2011

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