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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Detalles Bibliográficos
Autores principales: Cuccaro, Denis, Guarnaccia, Maria, Iemmolo, Rosario, D’Agata, Velia, Cavallaro, Sebastiano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128388/
https://www.ncbi.nlm.nih.gov/pubmed/30258280
http://dx.doi.org/10.2174/1389202919666180122141425

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128388/
https://www.ncbi.nlm.nih.gov/pubmed/30258280
http://dx.doi.org/10.2174/1389202919666180122141425

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