Mutation in saposin D domain of sphingolipid activator protein gene causes urinary system defects and cerebellar Purkinje cell degeneration with accumulation of hydroxy fatty acid-containing ceramide in mouse

Author: Matsuda Junko  

Publisher: Oxford University Press

E-ISSN: 0964-6906|13|21|2709-2723

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.13, Iss.21, 2004-11, pp. : 2709-2723

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