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Metachromatic leukodystrophy. Ultrastructural and enzymatic study of a case of variant O form

Archives of Neurology

Dec 1, 1975

Eric RaynaudRaphaël Lagarde

PMID: 985

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Abstract

A variant of metachromatic leukodystrophy (MLD), Austin disease, is characterized by a multiple isozyme deficiency of arylsulfatase. A 3 1/2-year-old girl with progressive mental and physical deterioration had decreased activities of arylsulfatases A and B in the leukocytes, shown by ac...read more

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  • Metachromatic leukodystrophy. Ultrastructural and enzymatic study of a case of variant O form

    Archives of Neurology

    Dec 1, 1975

    Eric RaynaudRaphaël Lagarde

    PMID: 985

    DOI:

    Abstract

    A variant of metachromatic leukodystrophy (MLD), Austin disease, is characterized by a multiple isozyme deficiency of arylsulfatase. A 3 1/2-year-old girl with progressive mental and physical deterioration had decreased activities of arylsulfatases A and B in the leukocytes, shown by ac...read more

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