[1]
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 (Aug. 2026), 628-638. DOI:https://doi.org/10.52852/tcncyh.v204i7.5535.