Clinical, Immunological, and Molecular Findings in Five Patients with Major Histocompatibility Complex Class II Deficiency from India-Reference-Cited by-同舟云学术

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Clinical, Immunological, and Molecular Findings in Five Patients with Major Histocompatibility Complex Class II Deficiency from India

Published:2018-02-16 Issue: Volume:9 Page:
ISSN:1664-3224
Container-title:Frontiers in Immunology
language:
Short-container-title:Front. Immunol.

Author:

Aluri Jahnavi,Gupta Maya,Dalvi Aparna,Mhatre Snehal,Kulkarni Manasi,Hule Gouri,Desai Mukesh,Shah Nitin,Taur Prasad,Vedam Ramprasad,Madkaikar Manisha

Publisher

Frontiers Media SA

Subject

Immunology,Immunology and Allergy

Reference22 articles.

1. Major histocompatibility class II expression deficiency caused by RFXANK founder mutation: a survey of 35 patients;Ouederni;Blood,2011

2. MHC class II deficiency: report of a novel mutation and special review;Farrokhi;Allergol Immunopathol (Madr),2017

3. MHC class I and II deficiencies;Hanna;J Allergy Clin Immunol,2014

4. Major histocompatibility complex class II deficiency: a clinical review;Elhasid;Blood Rev,1996

5. Complementation cloning of an MHC class I transactivator mutated in hereditary MHC class II deficiency (or bare lymphocyte syndrome);Steimle;Cell,1993

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