Phenotype of arylsulfatase A-deficient mice: Relationship to human metachromatic leukodystrophy

Metachromatic leukodystrophy is a lysosomal sphingolipid storage disorder caused by the deficiency of arylsulfatase A. The disease is characterized by progressive demyelination, causing various neurologic symptoms. Since no naturally occurring animal model of the disease is available, we have genera...

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Detalhes bibliográficos
Main Authors: Hess, Barbara, Saftig, Paul, Hartmann, Dieter, Coenen, Ruth, Lüllmann-Rauch, Renate, Goebel, Hans H., Evers, Meike, von Figura, Kurt, D’Hooge, Rudi, Nagels, Guy, De Deyn, Peter, Peters, Christoph, Gieselmann, Volkmar
Formato: Artigo
Idioma:Inglês
Publicado em: The National Academy of Sciences of the USA 1996
Assuntos:
Biological Sciences
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC26220/
https://ncbi.nlm.nih.gov/pubmed/8962139
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