Novel presentation of Omenn syndrome in association with aniridia-Reference-Cited by-同舟云学术

Novel presentation of Omenn syndrome in association with aniridia

Published:2009-04 Issue:4 Volume:123 Page:966-969
ISSN:0091-6749
Container-title:Journal of Allergy and Clinical Immunology
language:en
Short-container-title:Journal of Allergy and Clinical Immunology

Author:

Sheehan William J.,Delmonte Ottavia M.,Miller David T.,Roberts Amy E.,Bonilla Francisco A.,Morra Massimo,Giliani Silvia,Pai Sung-Yun,Notarangelo Luigi D.,Oettgen Hans C.

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference9 articles.

1. Partial V(D)J recombination activity leads to Omenn syndrome;Villa;Cell,1998

2. Mutations in the PAX6 gene in patients with hereditary aniridia;Davis;Hum Mol Genet,1993

3. Reviewing Omenn syndrome;Aleman;Eur J Pediatr,2001

4. V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations;Villa;Blood,2001

5. GvHD-associated cytokine polymorphisms do not associate with Omenn syndrome rather than T-B- SCID in patients with defects in RAG genes;Haq;Clin Immunol,2007

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