Duplication of exons 8–9 in NCF2 leading to incomplete clinical penetrance in Chronic Granulomatous Disease (2024)
- Authors:
- Autor USP: CONDINO NETO, ANTONIO - ICB
- Unidade: ICB
- DOI: 10.1007/s10875-023-01624-2
- Subjects: IMUNOLOGIA; DOENÇAS GENÉTICAS; MUTAÇÃO GENÉTICA; NEUTRÓFILOS; EXONS; OXIDAÇÃO
- Language: Inglês
- Imprenta:
- Publisher: Springer New York LLC
- Publisher place: New York
- Date published: 2024
- Source:
- Título: Journal of Clinical Immunology
- ISSN: 1573-2592
- Volume/Número/Paginação/Ano: v. 44, n. 1, 4 p., 2024
- Este artigo NÃO possui versão em acesso aberto
-
Status: Nenhuma versão em acesso aberto identificada -
ABNT
HERNANDEZ, Marco Antonio Venancio et al. Duplication of exons 8–9 in NCF2 leading to incomplete clinical penetrance in Chronic Granulomatous Disease. Journal of Clinical Immunology. New York: Springer New York LLC. Disponível em: https://doi.org/10.1007/s10875-023-01624-2. Acesso em: 13 mar. 2026. , 2024 -
APA
Hernandez, M. A. V., Flores, C. S., Juárez, M. J., Galicia, L. B., Espinosa-Padilla, S., & Condino Neto, A. (2024). Duplication of exons 8–9 in NCF2 leading to incomplete clinical penetrance in Chronic Granulomatous Disease. Journal of Clinical Immunology. New York: Springer New York LLC. doi:10.1007/s10875-023-01624-2 -
NLM
Hernandez MAV, Flores CS, Juárez MJ, Galicia LB, Espinosa-Padilla S, Condino Neto A. Duplication of exons 8–9 in NCF2 leading to incomplete clinical penetrance in Chronic Granulomatous Disease [Internet]. Journal of Clinical Immunology. 2024 ; 44( 1): 4 .[citado 2026 mar. 13 ] Available from: https://doi.org/10.1007/s10875-023-01624-2 -
Vancouver
Hernandez MAV, Flores CS, Juárez MJ, Galicia LB, Espinosa-Padilla S, Condino Neto A. Duplication of exons 8–9 in NCF2 leading to incomplete clinical penetrance in Chronic Granulomatous Disease [Internet]. Journal of Clinical Immunology. 2024 ; 44( 1): 4 .[citado 2026 mar. 13 ] Available from: https://doi.org/10.1007/s10875-023-01624-2 - Infecção por Blastomicose em pacientes com Hiper IgM ligada ao X (HIGM1)
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