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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Detalhes bibliográficos
Publicado no:Front Aging Neurosci
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2018
Assuntos:
Neuroscience
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5963122/
https://ncbi.nlm.nih.gov/pubmed/29867446
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnagi.2018.00136
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