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Chaperonopathies: Spotlight on Hereditary Motor Neuropathies
Distal hereditary motor neuropathies (dHMN) are a group of rare hereditary neuromuscular disorders characterized by an atrophy that affects peroneal muscles in the absence of sensory symptoms. To date, 23 genes are thought to be responsible for dHMN, four of which encode chaperones: DNAJB2, which en...
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| Publicat a: | Front Mol Biosci |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5155517/ https://ncbi.nlm.nih.gov/pubmed/28018906 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fmolb.2016.00081 |
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