A new alpha-synuclein missense variant (Thr72Met) in two Turkish families with Parkinson’s disease

INTRODUCTION: Missense variants and multiplications of the alpha-synuclein gene (SNCA) are established as rare causes of autosomal dominant forms of Parkinson’s Disease (PD). METHODS: Two families of Turkish origins with PD were studied; the SNCA coding region was analyzed by Sanger sequencing, and...

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Detalles Bibliográficos
Autores principales: Fevga, Christina, Park, Yangshin, Lohmann, Ebba, Kievit, Anneke J., Breedveld, Guido J., Ferraro, Federico, de Boer, Leon, van Minkelen, Rick, Hanagasi, Hasmet, Boon, Agnita, Wang, Wei, Petsko, Gregory A., Hoang, Quyen Q., Emre, Murat, Bonifati, Vincenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607441/
https://www.ncbi.nlm.nih.gov/pubmed/34229155
http://dx.doi.org/10.1016/j.parkreldis.2021.06.023

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607441/
https://www.ncbi.nlm.nih.gov/pubmed/34229155
http://dx.doi.org/10.1016/j.parkreldis.2021.06.023

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