C9orf72 Hexanucleotide Repeat in Huntington-Like Patients: Systematic Review and Meta-Analysis-Reference-Cited by-同舟云学术

C9orf72 Hexanucleotide Repeat in Huntington-Like Patients: Systematic Review and Meta-Analysis

Published:2020-11-02 Issue: Volume:11 Page:
ISSN:1664-8021
Container-title:Frontiers in Genetics
language:
Short-container-title:Front. Genet.

Author:

Alva-Diaz Carlos,Alarcon-Ruiz Christoper A.,Pacheco-Barrios Kevin,Mori Nicanor,Pacheco-Mendoza Josmel,Traynor Bryan J.,Rivera-Valdivia Andrea,Lertwilaiwittaya Pongtawat,Bird Thomas D.,Cornejo-Olivas Mario

Funder

National Institute on Aging

Publisher

Frontiers Media SA

Subject

Genetics (clinical),Genetics,Molecular Medicine

Reference44 articles.

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2. A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories;Akimoto;J. Med. Genet,2014

3. AromatarisE. MunnZ. 10.46658/JBIMES-20-01JBI Manual for Evidence Synthesis. JBI2020

4. The global prevalence of Huntington's disease: a systematic review and discussion;Baig;Neurodegener. Dis. Manag,2016

5. A study of Huntington disease-like syndromes in black South African patients reveals a single SCA2 mutation and a unique distribution of normal alleles across five repeat loci;Baine;J. Neurol. Sci,2018

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1. Recent advances in non-Huntington's disease choreas;Parkinsonism & Related Disorders;2024-05

2. C9ORF72 hexanucleotide repeat expansion: From ALS and FTD to a broader pathogenic role?;Revue Neurologique;2024-05

3. Genetics of Huntington’s disease and related disorders: beyond triplet repeats;Ageing and Neurodegenerative Diseases;2024-02-29

4. The repeat length of C9orf72 is associated with the survival of amyotrophic lateral sclerosis patients without C9orf72 pathological expansions;Frontiers in Neurology;2022-08-03

5. C9orf72 hexanucleotide repeat expansion found in suspected spinobulbar muscular atrophy (SBMA);Neurologia i Neurochirurgia Polska;2022-06-30