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An integrated approach for measuring copy number variation at the FCGR3 (CD16) locus
Copy number variation (CNV) is an important source of genomic diversity in humans, and influences disease susceptibility. The immunoglobulin-receptor genes FCGR3A and FCGR3B on chromosome 1q23.3 show CNV, and CNV of the FCGR3B gene is associated with glomerulonephritis in systemic lupus erythematosu...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2009
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3600569/ https://ncbi.nlm.nih.gov/pubmed/19143032 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.20911 |
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