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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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667021/
https://www.ncbi.nlm.nih.gov/pubmed/33240313
http://dx.doi.org/10.3389/fgene.2020.551780

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667021/
https://www.ncbi.nlm.nih.gov/pubmed/33240313
http://dx.doi.org/10.3389/fgene.2020.551780

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