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Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn’s disease
Following recent success in genome-wide association studies, a critical focus of human genetics is to understand how genetic variation at implicated loci influences cellular and disease processes. Crohn’s disease (CD) is associated with SNPs around IRGM1,2, but coding-sequence variation has been exc...
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| Main Authors: | , , , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2731799/ https://ncbi.nlm.nih.gov/pubmed/19165925 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.215 |
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