Neuronal loss in Pelizaeus–Merzbacher disease differs in various mutations of the proteolipid protein 1-Reference-Cited by-同舟云学术

Neuronal loss in Pelizaeus–Merzbacher disease differs in various mutations of the proteolipid protein 1

Published:2009-06-27 Issue:4 Volume:118 Page:531-539
ISSN:0001-6322
Container-title:Acta Neuropathologica
language:en
Short-container-title:Acta Neuropathol

Author:

Sima Anders A. F.,Pierson Christopher R.,Woltjer Randall L.,Hobson Grace M.,Golden Jeffrey A.,Kupsky William J.,Schauer Galen M.,Bird Thomas D.,Skoff Robert P.,Garbern James Y.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00401-009-0562-8.pdf

Reference45 articles.

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3. Boison D, Stoffel W (1994) Disruption of the compacted myelin sheath of axons of the central nervous system in proteolipid protein-deficient mice. Proc Natl Acad Sci USA 91:11709–11713

4. Bond C, Si X, Crisp M et al (1997) Family with Pelizaeus–Merzbacher disease/X-linked spastic paraplegia and a nonsense mutation in exon 6 of the proteolipid protein gene. Am J Med Genet 71:357–360

5. Boucher SE, Cypher MA, Carlock LR, Skoff RP (2002) Proteolipid protein gene modulates viability and phenotype of neurons. J Neurosci 22:1772–1783

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