Mutation of the proteolipid protein gene PLP in a human X chromosome-linked myelin disorder.
Myelin is a highly specialized membrane unique to the nervous system that ensheaths axons to permit the rapid saltatory conduction of impulses. The elaboration of a compact myelin sheath is disrupted in a diverse spectrum of human disorders, many of which are of unknown etiology. The X chromosome-li...
Gardado en:
| Publicado en: | Proc Natl Acad Sci U S A |
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| Principais autores: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
National Academy of Sciences
1989
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC298228/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2479017/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.86.20.8128 |
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