Phenotype of arylsulfatase A-deficient mice: Relationship to human metachromatic leukodystrophy-Reference-Cited by-同舟云学术

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

Published:1996-12-10 Issue:25 Volume:93 Page:14821-14826
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Hess B.,Saftig P.,Hartmann D.,Coenen R.,Lullmann-Rauch R.,Goebel H. H.,Evers M.,von Figura K.,D'Hooge R.,Nagels G.,De Deyn P.,Peters C.,Gieselmann V.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference23 articles.

1. Molecular genetics of metachromatic leukodystrophy

2. Molecular Basis of Different Forms of Metachromatic Leukodystrophy

3. Quantitative correlation between the residual activity of β-hexosaminidase A and arylsulfatase A and the severity of the resulting lysosomal storage disease

4. Structure of the Mouse Arylsulfatase A Gene and cDNA

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