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CNVs in Epilepsy
Copy number variants (CNVs) are deletions or duplications of DNA. CNVs have been increasingly recognized as an important source of both normal genetic variation and pathogenic mutation. Technologies for genome-wide discovery of CNVs facilitate studies of large cohorts of patients and controls to ide...
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| Autor principal: | |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer US
2014
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4129225/ https://ncbi.nlm.nih.gov/pubmed/25152848 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40142-014-0046-6 |
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