Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX array

Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX array

We have screened sporadic early-onset Alzheimer’s disease (sEOAD, n=408) samples using the NeuroX array for known causative and predicted pathogenic variants in 16 genes linked to familial forms of neurodegeneration. We found two sEOAD individuals harbouring a known causative variant in PARK2 known...

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Bibliographic Details
Main Authors: Barber, Imelda S., Braae, Anne, Clement, Naomi, Patel, Tulsi, Guetta-Baranes, Tamar, Brookes, Keeley, Medway, Christopher, Chappell, Sally, Guerreiro, Rita, Bras, Jose, Hernandez, Dena, Singleton, Andrew, Hardy, John, Mann, David M., Morgan, Kevin
Format: Article
Published: Elsevier 2017
Subjects:
Alzheimer's Disease
Parkinson's Disease
Sporadic
Early-onset
NeuroX
Screening
Online Access:https://eprints.nottingham.ac.uk/36987/

Internet

https://eprints.nottingham.ac.uk/36987/

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