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Non-coding genetic variants in human disease
Genetic variants, including single-nucleotide variants (SNVs) and copy number variants (CNVs), in the non-coding regions of the human genome can play an important role in human traits and complex diseases. Most of the genome-wide association study (GWAS) signals map to non-coding regions and potenti...
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| Publicat a: | Hum Mol Genet |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4572001/ https://ncbi.nlm.nih.gov/pubmed/26152199 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv259 |
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