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Interpreting Gene Expression Effects of Disease-Associated Variants: A Lesson from SNCA rs356168
The SNCA intronic single nucleotide polymorphism (SNP), rs356168, has been associated with Parkinson’s disease (PD) in large genome wide association studies (GWAS). Recently, the PD-risk allele, rs356168-G was shown to increase SNCA-mRNA expression using genome edited human induced pluripotent stem...
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| Veröffentlicht in: | Front Genet |
|---|---|
| Hauptverfasser: | , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Frontiers Media S.A.
2017
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5611418/ https://ncbi.nlm.nih.gov/pubmed/28979294 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2017.00133 |
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