My, P. T. T., Khánh, T. V., Tú, N. H., Dũng, V. C., Khánh, N. N., Lan, N. N., Phương, L. T., Thúy, N. T. P. and Tuấn, P. L. A. (2026) “Identification of SLC22A5 mutations and pedigree analysis in families of newborns suspected of primary Carnitine deficiency”, Journal of Medical Research, 204(7), pp. 628-638. doi: 10.52852/tcncyh.v204i7.5535.