Tvrdik T.,1998


Tvrdik T., Marcus S., Hou M.S., Falt S., Noori P., Podlutskaja N., Hanefeld F., Strome F., Lambert B. Molecular characterization of two deletion events involving Alu-sequences, one novel base substitution and two tentative hotsot mutations in the hypoxanthine guanine phosphoribosyltransferase (HPRT) gene in five patients with Lesch-Nyhan syndrome. - Hum.Genet., 1998, v. 10, p. 311-318.

鸯铗痂蝈 蜞赕:

  • HPRT 缅 (沐 汨镱犟囗蜩磴筻龛眙铖纛痂犷玷腧疣眈翦疣琨)