Prevalence of
Journal
Neurology. Genetics
ISSN: 2376-7839
Titre abrégé: Neurol Genet
Pays: United States
ID NLM: 101671068
Informations de publication
Date de publication:
Jun 2020
Jun 2020
Historique:
received:
07
11
2019
accepted:
15
03
2020
entrez:
26
6
2020
pubmed:
26
6
2020
medline:
26
6
2020
Statut:
epublish
Résumé
We evaluated the prevalence of pathogenic repeat expansions in replication factor C subunit 1 ( A cohort of 596 predominantly adult-onset patients with undiagnosed familial or sporadic cerebellar ataxia was evaluated at a tertiary referral ataxia center and excluded for common genetic causes of cerebellar ataxia. Patients were then screened for the presence of pathogenic repeat expansions in In the initial cohort, 41 samples were identified with 1 expanded allele in the In a large undiagnosed ataxia cohort from North America, biallelic pathogenic repeat expansion in
Identifiants
pubmed: 32582864
doi: 10.1212/NXG.0000000000000440
pii: NG2019012450
pmc: PMC7274910
doi:
Types de publication
Journal Article
Langues
eng
Pagination
e440Informations de copyright
Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.
Références
Handb Clin Neurol. 2018;147:105-123
pubmed: 29325606
Am J Hum Genet. 2019 Jul 3;105(1):151-165
pubmed: 31230722
Hum Mutat. 2020 Feb;41(2):487-501
pubmed: 31692161
JAMA Neurol. 2014 Oct;71(10):1237-46
pubmed: 25133958
Handb Clin Neurol. 2018;147:173-185
pubmed: 29325610
Nat Genet. 2019 Apr;51(4):649-658
pubmed: 30926972
Neurol Clin Pract. 2018 Feb;8(1):27-32
pubmed: 29517052
J Hum Genet. 2018 Sep;63(9):981-987
pubmed: 29891931
Am J Hum Genet. 2017 Jul 6;101(1):87-103
pubmed: 28686858
Handb Clin Neurol. 2018;147:187-209
pubmed: 29325611
Brain. 2018 Jul 1;141(7):1981-1997
pubmed: 29939198
Lancet Neurol. 2019 May;18(5):492-503
pubmed: 30981321
Genet Med. 2019 Jan;21(1):195-206
pubmed: 29915382