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Characterization of Parkinson’s disease-related pathogenic TMEM230 mutants
Parkinson’s disease (PD) is the second most common neurodegenerative disease. Although most PD cases are sporadic, 5–10% of them are hereditary and several pathogenic mutations in related genes have been identified. Mutations in TMEM230 were recently identified as a cause of autosomal dominant PD. H...
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| Publicado no: | Anim Cells Syst (Seoul) |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Taylor & Francis
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6138308/ https://ncbi.nlm.nih.gov/pubmed/30460091 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19768354.2018.1453545 |
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