Llwytho...
Perturbed Interactions of Mutant Proteolipid Protein/DM20 with Cholesterol and Lipid Rafts in Oligodendroglia: Implications for Dysmyelination in Spastic Paraplegia
Missense mutations in the human PLP1 gene lead to dysmyelinating diseases with a broad range of clinical severity, ranging from severe Pelizaeus–Merzbacher disease (PMD) to milder spastic paraplegia type 2 (SPG-2). The molecular pathology has been generally attributed to endoplasmic reticulum (ER) r...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | J Neurosci |
|---|---|
| Prif Awduron: | , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Society for Neuroscience
2006
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6674790/ https://ncbi.nlm.nih.gov/pubmed/17093095 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.3581-06.2006 |
| Tagiau: |
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