Clinical and genetic heterogeneity in Omenn syndrome and severe combined immune deficiency-Reference-Cited by-同舟云学术

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Clinical and genetic heterogeneity in Omenn syndrome and severe combined immune deficiency

Published:2009-03 Issue:2 Volume:13 Page:244-250
ISSN:1397-3142
Container-title:Pediatric Transplantation
language:en
Short-container-title:

Author:

Gruber Tanja A.,Shah Ami J.,Hernandez Michelle,Crooks Gay M.,Abdel-Azim Hisham,Gupta Sudhir,McKnight Sean,White Drew,Kapoor Neena,Kohn Donald B.

Publisher

Wiley

Subject

Transplantation,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3046.2008.00970.x/fullpdf

Reference18 articles.

1. Familial reticuloendotheliosis with eosinophilia;Omenn;N Engl J Med,1965

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

3. IL2RGbase: A database of γc-chain defects causing human X-SCID;Puck;Immunol Today,1996

4. Omenn’s syndrome occurring in patients without mutations in recombination activating genes;Gennery;Clin Immunol,2005

5. AIRE deficiency in thymus of 2 patients with Omenn syndrome;Cavadini;J Clin Invest,2005

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