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VPS35, the Retromer Complex and Parkinson’s Disease
Mutations in the vacuolar protein sorting 35 ortholog (VPS35) gene encoding a core component of the retromer complex, have recently emerged as a new cause of late-onset, autosomal dominant familial Parkinson’s disease (PD). A single missense mutation, AspD620Asn (D620N), has so far been unambiguousl...
Tallennettuna:
| Julkaisussa: | J Parkinsons Dis |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
IOS Press
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5438477/ https://ncbi.nlm.nih.gov/pubmed/28222538 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/JPD-161020 |
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