Whole-Exome Sequencing in Searching for New Variants Associated With the Development of Parkinson’s Disease

Background: Parkinson’s disease (PD) is a complex disease with its monogenic forms accounting for less than 10% of all cases. Whole-exome sequencing (WES) technology has been used successfully to find mutations in large families. However, because of the late onset of the disease, only small families...

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Detalles Bibliográficos
Autores principales: Shulskaya, Marina V., Alieva, Anelya Kh., Vlasov, Ivan N., Zyrin, Vladimir V., Fedotova, Ekaterina Yu., Abramycheva, Natalia Yu., Usenko, Tatiana S., Yakimovsky, Andrei F., Emelyanov, Anton K., Pchelina, Sofya N., Illarioshkin, Sergei N., Slominsky, Petr A., Shadrina, Maria I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5963122/
https://www.ncbi.nlm.nih.gov/pubmed/29867446
http://dx.doi.org/10.3389/fnagi.2018.00136

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5963122/
https://www.ncbi.nlm.nih.gov/pubmed/29867446
http://dx.doi.org/10.3389/fnagi.2018.00136

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