Identification of Disease-Associated Variants by Targeted Gene Panel Resequencing in Parkinson's Disease

Background: Recent advanced technologies, such as high-throughput sequencing, have enabled the identification of a broad spectrum of variants. Using targeted-gene-panel resequencing for Parkinson's disease (PD)-associated genes, we have occasionally found several single-nucleotide variants (SNV...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Front Neurol
Päätekijät: Daida, Kensuke, Funayama, Manabu, Li, Yuanzhe, Yoshino, Hiroyo, Hayashida, Arisa, Ikeda, Aya, Ogaki, Kotaro, Nishioka, Kenya, Hattori, Nobutaka
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Frontiers Media S.A. 2020
Aiheet:
Neurology
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7550729/
https://ncbi.nlm.nih.gov/pubmed/33117265
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2020.576465
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