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

Introduction: Patients with Huntington-Like disorders (HLD) comprise a variety of allelic disorders sharing a Huntington phenotype. The hexanucleotide repeat expansion of the C9orf72 gene could explain part of the HLD etiology. We aimed to conduct a systematic review and meta-analysis looking for th...

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Auteurs principaux:	Carlos Alva-Diaz, Christoper A. Alarcon-Ruiz, Kevin Pacheco-Barrios, Nicanor Mori, Josmel Pacheco-Mendoza, Bryan J. Traynor, Andrea Rivera-Valdivia, Pongtawat Lertwilaiwittaya, Thomas D. Bird, Mario Cornejo-Olivas
Format:	Artigo
Langue:	Inglês
Publié:	Frontiers Media S.A. 2020-11-01
Collection:	Frontiers in Genetics
Sujets:	C9orf72 Huntington like disorders systematic review chorea prevalence studies
Accès en ligne:	https://www.frontiersin.org/articles/10.3389/fgene.2020.551780/full
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