Authors:
Hulkova, H
Cervenkova, M
Ledvinova, J
Tochackova, M
Hrebicek, M
Poupetova, H
Befekadu, A
Berna, L
Paton, BC
Harzer, K
Boor, A
Smid, F
Elleder, M
Citation: H. Hulkova et al., 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 lactosylceramide accumulation, HUM MOL GEN, 10(9), 2001, pp. 927-940