NGỌC, C. T. B.; DŨNG, V. C. Utilization of whole exome sequencing to identify mutations of CYBB gene in patients with x-link chronic granulomatous disease . Journal of Medical Research, [S. l.], v. 138, n. 2, p. 19-27, 2021. DOI: 10.52852/tcncyh.v138i2.64. Disponível em: https://tapchinghiencuuyhoc.vn/index.php/tcncyh/article/view/64. Acesso em: 7 nov. 2026.