Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variant.
Pelizaeus-Merzbacher disease (PMD) is a human X chromosome-linked dysmyelination disorder of the central nervous system for which the genetic defect has not yet been established. The jimpy mutation jp of the mouse is an X chromosome-linked disorder of myelin formation. The mutation is at an intron/e...
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| Vydáno v: | Proc Natl Acad Sci U S A |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
1989
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC298509/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2480601/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.86.23.9427 |
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