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Autosomal dominant Parkinson’s disease caused by SNCA duplications
The discovery in 1997 that mutations in the SNCA gene cause Parkinson’s disease (PD) greatly advanced our understanding of this illness. There are pathogenic missense mutations and multiplication mutations in SNCA. Thus, not only a mutant protein, but also an increased dose of wild-type protein can...
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| 發表在: | Parkinsonism Relat Disord |
|---|---|
| Main Authors: | , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2015
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4820832/ https://ncbi.nlm.nih.gov/pubmed/26350119 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.parkreldis.2015.09.007 |
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