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The splice site variant rs11078928 may be associated with a genotype-dependent alteration in expression of GSDMB transcripts
BACKGROUND: Many genetic variants have been associated with susceptibility to complex traits by genome wide association studies (GWAS), but for most, causal genes and mechanisms of action have yet to be elucidated. Using bioinformatics, we identified index and proxy variants associated with autoimmu...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3848490/ https://ncbi.nlm.nih.gov/pubmed/24044605 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-14-627 |
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