Mendelian susceptibility to mycobacterial disease: 2014–2018 update-Reference-Cited by-同舟云学术

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Mendelian susceptibility to mycobacterial disease: 2014–2018 update

Published:2018-10-25 Issue:4 Volume:97 Page:360-367
ISSN:0818-9641
Container-title:Immunology & Cell Biology
language:en
Short-container-title:Immunol Cell Biol

Author:

Rosain Jérémie¹²³,Kong Xiao‐Fei⁴,Martinez‐Barricarte Ruben⁴,Oleaga‐Quintas Carmen¹²,Ramirez‐Alejo Noé⁴,Markle Janet⁴,Okada Satoshi⁴,Boisson‐Dupuis Stéphanie¹²⁴,Casanova Jean‐Laurent¹²⁴⁵⁶,Bustamante Jacinta¹²³⁴

Affiliation:

1. Laboratory of Human Genetics of Infectious Diseases Necker Branch INSERM UMR 1163 Necker Hospital for Sick Children Paris France

2. Imagine Institute Paris Descartes University Paris France

3. Study Center for Primary Immunodeficiencies AP‐HP Necker Children Hospital Paris France

4. St Giles Laboratory of Human Genetics of Infectious Diseases Rockefeller Branch Rockefeller University New York NY USA

5. Pediatric Hematology‐Immunology Unit Necker Hospital for Sick Children AP‐HP Paris France

6. Howard Hughes Medical Institute New York NY USA

Funder

Agence Nationale de la Recherche

National Institute of Allergy and Infectious Diseases

Stony Wold-Herbert Fund

Shanghai Educational Development Foundation

Consejo Nacional de Ciencia y Tecnología

Fonds de Recherche en Santé Respiratoire

Université Paris Descartes

St. Giles Foundation

Publisher

Wiley

Subject

Cell Biology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/imcb.12210

Reference71 articles.

1. Mendelian susceptibility to mycobacterial disease: Genetic, immunological, and clinical features of inborn errors of IFN-γ immunity

2. Inherited and acquired immunodeficiencies underlying tuberculosis in childhood

3. Autosomal Dominant IFN-γR1 Deficiency Presenting with both Atypical Mycobacteriosis and Tuberculosis in a BCG-Vaccinated South African Patient

4. Inherited IL‐12Rbeta1 deficiency in a child with BCG adenitis and oral candidiasis: a case report;Hatipoglu N;Pediatrics,2017

5. A digenic human immunodeficiency characterized by IFNAR1 and IFNGR2 mutations

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