TY  - INPR
N1  - © 2021 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association

This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
TI  - SORL1 mutation in a Greek family with Parkinson's disease and dementia
Y1  - 2021/09/10/
UR  - https://doi.org/10.1002/acn3.51433
A1  - Xiromerisiou, G
A1  - Bourinaris, T
A1  - Houlden, H
A1  - Lewis, PA
A1  - Senkevich, K
A1  - Hammer, M
A1  - Federoff, M
A1  - Khan, A
A1  - Spanaki, C
A1  - Hadjigeorgiou, GM
A1  - Bonstanjopoulou, S
A1  - Fidani, L
A1  - Ermolaev, A
A1  - Gan-Or, Z
A1  - Singleton, A
A1  - Vandrovcova, J
A1  - Hardy, J
JF  - Annals of Clinical and Translational Neurology
AV  - public
N2  - Whole exome sequencing and linkage analysis were performed in a three generational pedigree of Greek origin with a broad phenotypic spectrum spanning from Parkinson?s disease and Parkinson?s disease dementia to dementia of mixed type (Alzheimer disease and vascular dementia). We identified a novel heterozygous c.G1135T (p.G379W) variant in SORL1 which segregated with the disease in the family. Mutation screening in sporadic Greek PD cases identified one additional individual with the mutation, sharing the same 12.8Mb haplotype. Our findings provide support for SORL1 mutations resulting in a broad range of additional phenotypes and warrants further studies in neurodegenerative diseases beyond AD.
ID  - discovery10134756
ER  -