论文信息 - A founder mutation (R254X) of SLC22A5 (OCTN2) in Chinese primary carnitine deficiency patients - 字舞流文

A founder mutation (R254X) of SLC22A5 (OCTN2) in Chinese primary carnitine deficiency patients

W. Hwu | L. Law | N. Tang | L. Law | Rachel Chan | L. Fung | W. M. Zhang | L. Fung | Weimin Zhang | W.M. Zhang