Metachromatic leukodystrophy caused by a partial cerebroside sulfatase defect
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1982.tb00759.x/fullpdf
Reference34 articles.
1. Metachromatic form of diffuse cerebral sclerosis. I. Diagnosis during life by urine sediment examination;Austin;Neurology,1957
2. Metachromatic leukodystrophy (MLD). VIII. MLD in adults; diagnosis and pathogenesis;Austin;Arch. Neurol.,1968
3. The assay of arylsulphatases A and B in human urine;Baum;Clin. Chim. Acta,1959
4. Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts;Chang;Proc. nat. Acad. Sci. (Wash.),1980
5. Absence of ASA activity in healthy father of a patient with metachromatic leukodystrophy;Dubois;New Engl. J. Med.,1975
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