Genetic galactosylceramidase deficiency (Globoid cell leukodystrophy, Krabbe disease) in different mammalian species
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Molecular Biology
Link
http://link.springer.com/content/pdf/10.1007/BF02834075.pdf
Reference57 articles.
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3. Costantino-Ceccarini E., Fletcher T. F., and Suzuki K. (1976) Glycolipid metabolism in the canine form of globoid cell leukodystrophy. InCurrent Trends in Sphingolipidoses and Allied Disorders, edited by B.W. Volk and L. Schneck, Plenum Press, NY, pp. 127–145.
4. D’Agostino A.N., Sayre G. P., and Hagles A.B. (1963) Krabbe’s disease.Arch. Neurol. 8, 82–96.
5. Dawson G. (1973) Hepatic galactosylceramide in globoid cell leukodystrophy (Krabbe’s disease).Lipids 8, 154–156.
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