Gait Abnormalities and Progressive Myelin Degeneration in a New Murine Model of Pelizaeus-Merzbacher Disease with Tandem Genomic Duplication

Pelizaeus-Merzbacher disease (PMD) is a hypomyelinating leukodystrophy caused by mutations of the proteolipid protein 1 gene (PLP1), which is located on the X chromosome and encodes the most abundant protein of myelin in the central nervous sytem. Approximately 60% of PMD cases result from genomic d...

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Hoofdauteurs: Clark, Kristi, Sakowski, Lauren, Sperle, Karen, Banser, Linda, Landel, Carlisle P., Bessert, Denise A., Skoff, Robert P., Hobson, Grace M.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Society for Neuroscience 2013
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Articles
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3713721/
https://ncbi.nlm.nih.gov/pubmed/23864668
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.1336-13.2013
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