Deletion of the entire interferon-γ receptor 1 gene causing complete deficiency in three related patients-Reference-Cited by-同舟云学术

Deletion of the entire interferon-γ receptor 1 gene causing complete deficiency in three related patients

Published:2016-03-01 Issue:3 Volume:36 Page:195-203
ISSN:0271-9142
Container-title:Journal of Clinical Immunology
language:en
Short-container-title:J Clin Immunol

Author:

de Vor Inge C.,van der Meulen Pomme M.,Bekker Vincent,Verhard Els M.,Breuning Martijn H.,Harnisch Esther,van Tol Maarten J. D.,Wieringa Jantien W.,van de Vosse Esther,Bredius Robbert G. M.

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy

Link

http://link.springer.com/content/pdf/10.1007/s10875-016-0244-y.pdf

Reference45 articles.

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2. van de Vosse E, van Dissel JT, Ottenhoff TH. Genetic deficiencies of innate immune signalling in human infectious disease. Lancet Infect Dis. 2009;9(11):688–98.

3. Dorman SE, Picard C, Lammas D, Heyne K, Van Dissel JT, Baretto R, et al. Clinical features of dominant and recessive interferon gamma receptor 1 deficiencies. Lancet. 2004;364(9451):2113–21.

4. Camcioglu Y, Picard C, Lacoste V, Dupuis S, Akcakaya N, Cokura H, et al. HHV-8-associated Kaposi sarcoma in a child with IFNgammaR1 deficiency. J Pediatr. 2004;144(4):519–23.

5. Taramasso L, Boisson-Dupuis S, Garre ML, Bondi E, Cama A, Nozza P, et al. Pineal germinoma in a child with interferon-gamma receptor 1 deficiency. case report and literature review. J Clin Immunol. 2014;34(8):922–7.

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