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TAP deficiency syndrome

Published:2000-08 Issue:2 Volume:121 Page:173-178
ISSN:1365-2249
Container-title:Clinical and Experimental Immunology
language:en
Short-container-title:

Author:

Gadola S D¹,Moins-Teisserenc H T¹²,Trowsdale J³,Gross W L⁴,Cerundolo V¹

Affiliation:

1. Institute of Molecular Medicine, Nuffield Department of Medicine, Oxford, UK

2. Institut Universitaire d'Hematologie, Unite INSERM U396, Hopital Saint-Louis, Paris, France

3. Cambridge University, Department of Pathology, Immunology Division, Cambridge, UK

4. Rheumaklinik Bad Bramstedt, University of Lübeck, Bad Bramstedt, Germany

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

Link

https://academic.oup.com/cei/article-pdf/121/2/173/42130220/j.1365-2249.2000.01264.x.pdf

Reference52 articles.

1. Combined immunodeficiency disease associated with absence of cell surface HLA-A and B antigens;Touraine;J Pediatr,1978

2. Association of a syndrome resembling Wegener's granulomatosis with low surface expression of HLA class I-molecules;Moins-Teisserenc;Lancet,1999

3. A case of primary immunodeficiency due to a defect of the major histocompatibility gene complex class I processing and presentation pathway;Teisserenc;Immunol Letters,1997

4. Homozygous human TAP peptide transporter mutation in HLA class I deficiency;De la Salle;Science,1994

5. Association of HLA class I antigen deficiency related to a TAP2 gene mutation with familial bronchiectasis;Donato;J Pediatr,1995

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