Genetic, Immunological, and Clinical Features of 32 Patients with Autosomal Recessive STAT1 Deficiency-Reference-Cited by-同舟云学术

Genetic, Immunological, and Clinical Features of 32 Patients with Autosomal Recessive STAT1 Deficiency

Published:2021-06-28 Issue:1 Volume:207 Page:133-152
ISSN:0022-1767
Container-title:The Journal of Immunology
language:en
Short-container-title:J.I.

Author:

Le Voyer Tom,Sakata Sonoko,Tsumura Miyuki,Khan Taushif^ORCID,Esteve-Sole Ana^ORCID,Al-Saud Bandar K.,Gungor Hatice Eke^ORCID,Taur Prasad,Jeanne-Julien Valentine,Christiansen Mette^ORCID,Köhler Lisa-Maria,ElGhazali Gehad Eltayeb,Rosain Jérémie^ORCID,Nishimura Shiho,Sakura Fumiaki,Bouaziz Matthieu,Oleaga-Quintas Carmen^ORCID,Nieto-Patlán Alejandro^ORCID,Deyà-Martinez Àngela,Altuner Torun Yasemin,Neehus Anna-Lena^ORCID,Roynard Manon^ORCID,Bozdemir Sefika Elmas,Al Kaabi Nawal^ORCID,Al Hassani Moza,Mersiyanova Irina^ORCID,Rozenberg Flore,Speckmann Carsten,Hainmann Ina,Hauck Fabian^ORCID,Alzahrani Mohammed Hamdan,Alhajjar Sami Hussain^ORCID,Al-Muhsen Saleh,Cole Theresa^ORCID,Fuleihan Ramsay,Arkwright Peter D.^ORCID,Badolato Raffaele,Alsina Laia^ORCID,Abel Laurent,Desai Mukesh,Al-Mousa Hamoud,Shcherbina Anna^ORCID,Marr Nico,Boisson-Dupuis Stéphanie,Casanova Jean-Laurent,Okada Satoshi,Bustamante Jacinta

Publisher

The American Association of Immunologists

Subject

Immunology,Immunology and Allergy

Reference73 articles.

1. Impaired response to interferon-α/β and lethal viral disease in human STAT1 deficiency

2. Inborn errors of human STAT1: allelic heterogeneity governs the diversity of immunological and infectious phenotypes

3. A novel presentation of homozygous loss-of-function STAT-1 mutation in an infant with hyperinflammation-A case report and review of the literature.;Burns;J. Allergy Clin. Immunol. Pract.,2016

4. Human Complete Stat-1 Deficiency Is Associated with Defective Type I and II IFN Responses In Vitro but Immunity to Some Low Virulence Viruses In Vivo

5. Long-term survival after hematopoietic stem cell transplantation for complete STAT1 deficiency.;Naviglio;J. Clin. Immunol.,2017

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