Author:
Sevin C,Verot L,Benraiss A,Van Dam D,Bonnin D,Nagels G,Fouquet F,Gieselmann V,Vanier M T,De Deyn P P,Aubourg P,Cartier N
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,Molecular Medicine
Reference40 articles.
1. von Figura K, Gieselmann V, Jaeken J . Metachromatic leukodystrophy. In: Scriver CR, Beaudet AL, Sly WS and Valle D (eds). The Metabolic & Molecular Bases of Inherited Disease, 8th edn, McGraw-Hill Published: New York, 2001, pp 3695–3724.
2. Dupree JL, Popko B . Genetic dissection of myelin galactolipid function. J Neurocytol 1999; 28: 271–279.
3. Pernber Z, Molander-Melin M, Berthold CH, Hansson E, Fredman P . Expression of the myelin and oligodendrocyte progenitor marker sulfatide in neurons and astrocytes of adult rat brain. J Neurosci Res 2002; 69: 86–93.
4. Molander-Melin M, Pernber Z, Franken S, Gieselmann V, Mansson JE, Fredman P . Accumulation of sulfatide in neuronal and glial cells of arylsulfatase A deficient mice. J Neurocytol 2004; 33: 417–427.
5. Hess B, Saftig P, Hartmann D, Coenen R, Lullmann-Rauch R, Goebel HH et al. Phenotype of arylsulfatase A-deficient mice: relationship to human metachromatic leukodystrophy. Proc Natl Acad Sci USA 1996; 93: 14821–14826.
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