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...
Kaydedildi:
| Yayımlandı: | Proc Natl Acad Sci U S A |
|---|---|
| Asıl Yazarlar: | , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
National Academy of Sciences
1989
|
| Konular: | |
| Online Erişim: | 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 |
| Etiketler: |
Etiket eklenmemiş, İlk siz ekleyin!
|