Phenotypic variability and neuropsychological findings associated with C9orf72 repeat expansions in a Bulgarian dementia cohort-Reference-Cited by-同舟云学术

Phenotypic variability and neuropsychological findings associated with C9orf72 repeat expansions in a Bulgarian dementia cohort

Published:2018-12-14 Issue:12 Volume:13 Page:e0208383
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Mehrabian Shima,Thonberg Håkan,Raycheva Margarita,Lilius Lena,Stoyanova Katya,Forsell Charlotte^ORCID,Cavallin Lena,Nesheva Desislava,Westman Eric,Toncheva Draga,Traykov Latchezar,Winblad Bengt,Graff Caroline

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference84 articles.

1. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD;AE Renton;Neuron,2011

2. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS;M DeJesus-Hernandez;Neuron,2011

3. A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study;I Gijselinck;Lancet Neurol,2012

4. The Genetics of C9orf72 Expansions;I Gijselinck;Cold Spring Harb Perspect Med,2017

5. Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion;BK Khan;J Neurol Neurosurg Psychiatry,2012

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Theme 02 - Genetics and Genomics;Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration;2023-11-06

2. Young Onset Alzheimer’s Disease Associated with C9ORF72 Hexanucleotide Expansion: Further Evidence for a Still Unsolved Association;Genes;2023-04-17

3. Targeted Screening of the C9orf72 Gene in Bulgarian Amyotrophic Lateral Sclerosis Patients;Acta Medica Bulgarica;2022-04-01

4. Dysgraphic features in motor neuron disease: a review;Aphasiology;2021-06-21

5. Dysgraphic features in motor neuron disease: a review;2021-02-01