Metachromatic leukodystrophy in Greece: observations on 4 cases
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1990.tb03387.x/fullpdf
Reference15 articles.
1. Metachromatic sulphatides in cerebral white matter and kidney;Austin;Proc. Sac. Biol. Med.,1959
2. A controlled study of enzym-ic activities in three human disorders of glycoli-pid metabolism;Austin;J. Neurochem.,1963
3. The assay of arylsulphatase A and B in human urine;Baum;Clin. Chim. Acta,1959
4. Multiple molecular forms of arylsulphatase A in different forms of metachromatic leukodystrophy (MLD);Farrell;Neurology,1979
5. Cerebroside sulphate hydrolysis by fibroblasts from a metachromatic leukodystrophy parent with deficient arylsulphatase A;Fluharty;J. Pediatr.,1978
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