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Parkinson's disease‐linked V15A mutation facilitates α‐synuclein aggregation by reducing membrane affinity
Parkinson's disease can manifest either as a sporadic form, which is common, or as an inherited autosomal dominant trait resulting from missense mutations. Recently, the novel α‐synuclein variant V15A was identified in two Caucasian and two Japanese families with Parkinson's disease. Using...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley & Sons, Inc.
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357493/ https://www.ncbi.nlm.nih.gov/pubmed/37358478 http://dx.doi.org/10.1002/pro.4693 |