The use of natural and artificial substrates in the prenatal diagnosis of Krabbe's disease
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01805686
Reference13 articles.
1. Besley, G. T. N. and Bain, A. D. (1976). Krabbe's globoid cell leucodystrophy. Studies on galactosylceramideβ-galactosidase and non-specificβ-galactosidase of leucocytes, cultured skin fibroblasts and amniotic fluid cells.J. Med. Genet.,13, 195
2. Besley, G. T. N. and Broadhead, D. M. (1976). Studies on humanN-acetyl-β-D-hexosaminidase C separated from neonatal brain.Biochem. J.,155, 205
3. Gal, A. E., Brady, R. O., Hibbert, S. R. and Pentchev, P. G. (1975). A practical chromogenic procedure for the detection of homozygotes and heterozygous carriers in Niemann-Pick disease.N. Engl. J. Med.,293, 632
4. Gal, A. E., Brady, R. O., Pentchev, P. G., Furbish, F. S., Suzuki, K., Tanaka, H. and Schneider, E. L. (1977). A practical chromogenic procedure for the diagnosis of Krabbe's disease.Clin. Chim. Acta,77, 53
5. Harzer, K., Benz, H. U., Knörr-Gärtner, H., Jonathan, W. D. and Knörr, K. (1976). Pränatale diagnose der globoidzell-leukodystrophie (Morbus Krabbe).Dtsch. Med. Wochenschr.,101, 821
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4. Use of Mixed Dispersion of Fluorescent Galactosylceramide and Sodium Dodecylsulfate for Assaying Galactosylceramide-β-Galactosidase and Diagnosing Krabbe Disease;Enzyme;1985
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