Second Report of Chronic Granulomatous Disease in Jordan: Clinical and Genetic Description of 31 Patients From 21 Different Families, Including Families From Lybia and Iraq.
Jordan
NADPH oxidase
autosomal recessive
chronic granulomatous disease
founder mutation
innate immunodeficiency
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2021
2021
Historique:
received:
08
12
2020
accepted:
08
02
2021
entrez:
22
3
2021
pubmed:
23
3
2021
medline:
22
9
2021
Statut:
epublish
Résumé
Chronic granulomatous Disease (CGD) is a rare innate immunodeficiency disorder caused by mutations in one of the six genes (
Identifiants
pubmed: 33746979
doi: 10.3389/fimmu.2021.639226
pmc: PMC7973097
doi:
Substances chimiques
Superoxides
11062-77-4
NADPH Oxidases
EC 1.6.3.-
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
639226Informations de copyright
Copyright © 2021 Bakri, Mollin, Beaumel, Vigne, Roux-Buisson, Al-Wahadneh, Alzyoud, Hayajneh, Daoud, Shukair, Karadshe, Sarhan, Al-Ramahi, Fauré, Rendu and Stasia.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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