Novel Diagnostic Tool for p47phox-Deficient Chronic Granulomatous Disease Patient and Carrier Detection
Chronic granulomatous disease (CGD) is a primary immunodeficiency caused by mutations of the phagocytic nicotinamide adenine dinucleotide phosphate (NADPH) oxidase. Autosomal recessive p47phox-deficient CGD (p47phox CGD) is the second most frequent form of the disease in western countries, and more...
Gardado en:
| Principais autores: | , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Elsevier
2019-06-01
|
| Series: | Molecular Therapy: Methods & Clinical Development |
| Acceso en liña: | http://www.sciencedirect.com/science/article/pii/S232905011930018X |
| Tags: |
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|