The gene coding for a sphingolipid activator protein, SAP-1, is on human chromosome 10
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00293023.pdf
Reference20 articles.
1. Fujibayashi S, Inui K, Wenger DA (1984) Activator protein deficient metachromatic leukodystrophy: Diagnosis in leukocytes using immunologic methods. J Pediatr 104:739?742
2. Inui K, Wenger DA (1982) Properties of a protein activator of glycosphingolipid hydrolysis isolated from the liver of a patient with GM1 gangliosidosis, Type 1. Biochem Biophys Res Commun 105:745?751
3. Inui K, Wenger DA (1983) Concentrations of an activator protein for sphingolipid hydrolysis in liver and brain samples from patients with lysosomal storage diseases. J Clin Invest 72:1622?1628
4. Inui K, Wenger DA (1984): Biochemical, immunological, and structural studies on a sphingolipid activator protein (SAP-1). Arch Biochem Biophys 233:556?564
5. Inui K, Emmett M, Wenger DA (1983) Immunological evidence for a deficiency in an activator protein for sulfatide sulfatase in a variant form of metachromatic leukodystrophy. Proc Natl Acad Sci USA 80:3074?3077
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