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My PTT, Khánh TV, Tú NH, Dũng VC, Khánh NN, Lan NN, Phương LT, Thúy NTP, Tuấn PLA. Identification of SLC22A5 mutations and pedigree analysis in families of newborns suspected of primary Carnitine deficiency. TCNCYH [Internet]. 2026Aug.4 [cited 2026Nov.8];204(7):628-3. Available from: https://tapchinghiencuuyhoc.vn/index.php/tcncyh/article/view/5535