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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Bibliografske podrobnosti

izdano v:	Proc Natl Acad Sci U S A
Principais autores:	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
Format:	Artigo
Jezik:	Inglês
Izdano:	National Academy of Sciences 1996
Teme:	Biological Sciences
Online dostop:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC26220/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8962139/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.93.25.14821
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