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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 no: | Curr Genomics |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Bentham Science Publishers
2018
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| Assuntos: | |
| Acesso em linha: | 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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