A novel mutation in the coding region of the prosaposin gene leads to a complete deficiency of prosaposin and saposins, and is associated with a complex sphingolipidosis dominated... by HULKOVA, H, CERVENKOVA, M, BÖÖR, A, SMID, F, ELLEDER, M, LEDVINOVA, J, TOCHACKOVA, M, HREBICEK, M, POUPETOVA, H, BEFEKADU, A, BERNA, L, PATON, B. C, HARZER, K

Get full text