Deletion of a splicing enhancer disrupts PLP1/DM20 ratio and myelin stability-Reference-Cited by-同舟云学术

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Deletion of a splicing enhancer disrupts PLP1/DM20 ratio and myelin stability

Published:2008-12 Issue:2 Volume:214 Page:322-330
ISSN:0014-4886
Container-title:Experimental Neurology
language:en
Short-container-title:Experimental Neurology

Author:

Wang Erming,Dimova Neviana,Sperle Karen,Huang Zhong,Lock Leslie,McCulloch Mailis C.,Edgar Julia M.,Hobson Grace M.,Cambi Franca

Publisher

Elsevier BV

Subject

Developmental Neuroscience,Neurology

Reference36 articles.

1. Genetic background determines phenotypic severity of the Plp rumpshaker mutation;Al-Saktawi;J. Neurosci. Res.,2003

2. PLP1 splicing abnormalities identified in Pelizaeus-Merzbacher disease and SPG2 fibroblasts are associated with different types of mutations;Bonnet-Dupeyron;Hum. Mutat.,2008

3. Genotype–phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations;Cailloux;Eur. J. Hum. Genet.,2000

4. Cellular and molecular aspects of myelin protein gene expression;Campagnoni;Mol. Neurobiol.,1988

5. Axonal loss in multiple sclerosis: a pathological survey of the corticospinal and sensory tracts;DeLuca;Brain,2004

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