Kuchař, L., Ledvinová, J., Hřebíček, M., Myšková, H., Dvořáková, L., Berná, L., . . . Harzer, K. (2009). Prosaposin Deficiency and Saposin B Deficiency (Activator-Deficient Metachromatic Leukodystrophy): Report on Two Patients Detected by Analysis of Urinary Sphingolipids and Carrying Novel PSAP Gene Mutations. Wiley Subscription Services, Inc., A Wiley Company.
Chicago-tyylinen lähdeviittausKuchař, Ladislav, et al. Prosaposin Deficiency and Saposin B Deficiency (Activator-Deficient Metachromatic Leukodystrophy): Report On Two Patients Detected By Analysis of Urinary Sphingolipids and Carrying Novel PSAP Gene Mutations. Wiley Subscription Services, Inc., A Wiley Company, 2009.
MLA-viiteKuchař, Ladislav, et al. Prosaposin Deficiency and Saposin B Deficiency (Activator-Deficient Metachromatic Leukodystrophy): Report On Two Patients Detected By Analysis of Urinary Sphingolipids and Carrying Novel PSAP Gene Mutations. Wiley Subscription Services, Inc., A Wiley Company, 2009.