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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Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Front Aging Neurosci
Päätekijät: 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.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Frontiers Media S.A. 2018
Aiheet:
Neuroscience
Linkit: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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