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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...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Veröffentlicht in:Curr Genomics
Hauptverfasser: Cuccaro, Denis, Guarnaccia, Maria, Iemmolo, Rosario, D’Agata, Velia, Cavallaro, Sebastiano
Format: Artigo
Sprache:Inglês
Veröffentlicht: Bentham Science Publishers 2018
Schlagworte:
Online Zugang: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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