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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...
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| Vydáno v: | Front Neurol |
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| Hlavní autoři: | , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Frontiers Media S.A.
2020
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| Témata: | |
| On-line přístup: | 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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