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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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| Vydáno v: | Front Pediatr |
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| Hlavní autoři: | , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Frontiers Media S.A.
2019
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| 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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