| Literature DB >> 29376855 |
Estrella Gómez-Tortosa1, María Ruggiero1, Ma José Sainz1, Alberto Villarejo-Galende2, Cristina Prieto-Jurczynska3, Begoña Venegas Pérez3, Carlos Ordás3, Pablo Agüero1, Rosa Guerrero-López4, Julián Pérez-Pérez5.
Abstract
The SORL1 gene encodes a protein involved in the amyloidogenic process, and its variants have been associated with Alzheimer's disease (AD) physiopathology. We screened for SORL1 variants in 124 familial (44 early- and 80 late-onset) dementia of Alzheimer type (DAT) cases. Nine potentially pathogenic changes (three not previously reported and six rare variants) were found in nine probands (7%). After screening the control population and siblings (presence in at least 1/200 controls and/or absence of segregation pattern), a causal relationship with the disease was considered unlikely in six variants and uncertain in one. The change Trp848Ter and a splice-site variant remained likely correlated with the disease. SORL1 mutations are present in 7% of our familial DAT cohort, though in most cases cannot be considered the direct cause of the disease.Entities:
Keywords: Alzheimer’s disease; SORL1 gene; SORLA protein; familial; neurogenetics
Mesh:
Substances:
Year: 2018 PMID: 29376855 DOI: 10.3233/JAD-170590
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472