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Animal models for inherited peripheral neuropathies
Recent progress in human genetics and neurobiology has led to the identification of various mutations in particular myelin genes as the cause for many of the known inherited demyelinating peripheral neuropathies. Mutations in 3 distinct myelin genes, PMP22, P(0), and connexin 32 cause the 3 major de...
Tallennettuna:
| Päätekijä: | |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
1997
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1467690/ https://ncbi.nlm.nih.gov/pubmed/9418989 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1046/j.1469-7580.1997.19130321.x |
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