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Whole-genome detection of disease-associated deletions or excess homozygosity in a case–control study of rheumatoid arthritis
Unlike genome-wide association studies, few comprehensive studies of copy number variation's contribution to complex human disease susceptibility have been performed. Copy number variations are abundant in humans and represent one of the least well-studied classes of genetic variants; in additi...
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| Autori principali: | , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2013
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3578409/ https://ncbi.nlm.nih.gov/pubmed/23223014 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/dds512 |
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