Premature termination codon mutations in ABCA7 contribute to Alzheimer's disease risk in Belgian patients.

The ATP-Binding Cassette Subfamily A Member 7 gene (ABCA7) was identified as a risk gene for Alzheimer's disease (AD) in genome-wide association studies of large cohorts of late-onset AD (LOAD) patients. Extended resequencing of the ABCA7 coding regions identified mutations that lead to premature termination codons (PTC) and loss of function of ABCA7. PTC mutations were enriched in LOAD patients and were frequently present in patients with early-onset AD (EOAD). We aimed at assessing the contribution of ABCA7 PTC mutations to AD in the Belgian population by screening the ABCA7 coding region in... Mehr ...

Verfasser: Bossaerts, Liene
Hens, Elisabeth
Hanseeuw, Bernard
Vandenberghe, Rik
Cras, Patrick
De Deyn, Peter P
Engelborghs, Sebastiaan
Van Broeckhoven, Christine
BELNEU Consortium
Dokumenttyp: Artikel
Erscheinungsdatum: 2021
Verlag/Hrsg.: Elsevier
Schlagwörter: ABCA7 / Alzheimer's disease / Loss-of function / PTC mutations / Premature termination codon
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-28490277
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : http://hdl.handle.net/2078.1/253774