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NeuroArray, A Custom CGH Microarray to Decipher Copy Number Variants in Alzheimer’s Disease
BACKGROUND: Copy Number Variants (CNVs) represent a prevailing type of structural variation (deletions or duplications) in the human genome. In the last few years, several studies have demonstrated that CNVs represent significant mutations in Alzheimer’s Disease (AD) hereditability. Currently, innov...
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| Publicado en: | Curr Genomics |
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| Autores principales: | , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Bentham Science Publishers
2018
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6128388/ https://ncbi.nlm.nih.gov/pubmed/30258280 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/1389202919666180122141425 |
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