Studies on a sphingolipid activator protein ( SAP-2) in fibroblasts from patients with lysosomal storage diseases, including Niemann-Pick disease Type C

Author:

Fujibayashi Shinsuke,Wenger David A.

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference24 articles.

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2. Gaucher's disease: deficiency of ‘acid’ β-glucosidase and reconstitution of enzyme activity in vitro;Ho,1971

3. An activator stimulating the enzymic hydrolysis of sphingolipids;Li;J Biol Chem,1976

4. Studies on the sphingolipid activator protein for the enzymatic hydrolysis of GM1 ganglioside and sulfatide;Wenger,1984

5. AB variant of infantile Gm2 gangliosidosis. Deficiency of a factor necessary for stimulation of hexosaminidase A-catalyzed degradation of ganglioside GM2 and glycolipid ga2;Conzelmann,1978

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