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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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| Vydáno v: | Curr Genomics |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Bentham Science Publishers
2018
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| Témata: | |
| On-line přístup: | 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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