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A Novel Mutation in the NCF2 Gene in a CGD Patient With Chronic Recurrent Pneumopathy

Chronic granulomatous disease (CGD) is an inherited, genetically heterogeneous disease characterized by defective phagocytic cell microbicidal function, leading to increased susceptibility to bacterial and fungal infections. CGD is caused by mutations in components of the nicotinamide adenine dinucl...

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Podrobná bibliografie
Vydáno v:Front Pediatr
Hlavní autoři: de Albuquerque, Jose Antonio Tavares, Lima, Alessandra Miramontes, de Oliveira Junior, Edgar Borges, Ishizuka, Edson Kiyotaka, Aragão-Filho, Walmir Cutrim, Bengala Zurro, Nuria, Mayumi Chiba, Sônia, Fernandes, Fátima Rodrigues, Condino-Neto, Antonio
Médium: Artigo
Jazyk:Inglês
Vydáno: Frontiers Media S.A. 2019
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6776604/
https://ncbi.nlm.nih.gov/pubmed/31612120
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2019.00391
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