A novel human primary immunodeficiency syndrome caused by deficiency of the endosomal adaptor protein p14-Reference-Cited by-同舟云学术

A novel human primary immunodeficiency syndrome caused by deficiency of the endosomal adaptor protein p14

Published:2006-12-31 Issue:1 Volume:13 Page:38-45
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Bohn Georg,Allroth Anna,Brandes Gudrun,Thiel Jens,Glocker Erik,Schäffer Alejandro A,Rathinam Chozhavendan,Taub Nicole,Teis David,Zeidler Cornelia,Dewey Ricardo A,Geffers Robert,Buer Jan,Huber Lukas A,Welte Karl,Grimbacher Bodo,Klein Christoph

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/nm1528.pdf

Reference42 articles.

1. Fischer, A. Human primary immunodeficiency diseases: a perspective. Nat. Immunol. 5, 23–30 (2004).

2. Stinchcombe, J., Bossi, G. & Griffiths, G.M. Linking albinism and immunity: the secrets of secretory lysosomes. Science 305, 55–59 (2004).

3. Barbosa, M.D.F.S. et al. Identification of the homologous beige and Chediak-Higashi syndrome genes. Nature 382, 262–265 (1996).

4. Nagle, D.L. et al. Identification and mutation analysis of the complete gene for Chediak-Higashi syndrome. Nat. Genet. 14, 307–311 (1996).

5. Klein, C. et al. Partial albinism with immunodeficiency (Griscelli syndrome). J. Pediatr. 125, 886–895 (1994).

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