A novel mutation in the NCF2 gene in a CGD patient with chronic recurrent pneumopathy (2019)
Source: Frontiers in Pediatrics. Unidade: ICB
Subjects: DOENÇAS GENÉTICAS, FAGÓCITOS, MUTAÇÃO GENÉTICA, IMUNOGENÉTICA, INFECÇÕES BACTERIANAS E MICOSES, SEQUENCIAMENTO GENÉTICO
ABNT
ALBUQUERQUE, José Antônio Tavares de et al. A novel mutation in the NCF2 gene in a CGD patient with chronic recurrent pneumopathy. Frontiers in Pediatrics, v. 7, p. 1-5, 2019Tradução . . Disponível em: https://doi.org/10.3389/fped.2019.00391. Acesso em: 20 out. 2024.APA
Albuquerque, J. A. T. de, Lima, A. M., Oliveira Junior, E. B. de, Ishizuka, E. K., Aragão-Filho, W. C., Zurro, N. B., et al. (2019). A novel mutation in the NCF2 gene in a CGD patient with chronic recurrent pneumopathy. Frontiers in Pediatrics, 7, 1-5. doi:10.3389/fped.2019.00391NLM
Albuquerque JAT de, Lima AM, Oliveira Junior EB de, Ishizuka EK, Aragão-Filho WC, Zurro NB, Chiba SM, Fernandes FR, Condino Neto A. A novel mutation in the NCF2 gene in a CGD patient with chronic recurrent pneumopathy [Internet]. Frontiers in Pediatrics. 2019 ; 7 1-5.[citado 2024 out. 20 ] Available from: https://doi.org/10.3389/fped.2019.00391Vancouver
Albuquerque JAT de, Lima AM, Oliveira Junior EB de, Ishizuka EK, Aragão-Filho WC, Zurro NB, Chiba SM, Fernandes FR, Condino Neto A. A novel mutation in the NCF2 gene in a CGD patient with chronic recurrent pneumopathy [Internet]. Frontiers in Pediatrics. 2019 ; 7 1-5.[citado 2024 out. 20 ] Available from: https://doi.org/10.3389/fped.2019.00391