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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Dettagli Bibliografici
Pubblicato in:Front Aging Neurosci
Autori principali: 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.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Frontiers Media S.A. 2018
Soggetti:
Neuroscience
Accesso online: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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