Non-coding repeat analyses in patients with Parkinson’s disease

Non-coding repeat analyses in patients with Parkinson’s disease

IntroductionThe genetic etiology of Parkinson’s disease (PD) is complex; approximately 10% of patients with PD have various gene mutations that lead to familial forms of the disease. Recent analyses of non-coding repeat regions revealed that many neurodegenerative diseases are associated with pathol...

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Main Authors: Makito Hirano, Makoto Samukawa, Satoko Miyatake, Yuko Yamagishi, Chiharu Isono, Rino Yoshikawa, Kazumasa Saigoh, Atsushi Terayama, Yuji Higashimoto, Eriko Koshimizu, Takeshi Mizuguchi, Kanako Fujii, Yoshiyuki Mitsui, Naomichi Matsumoto, Yoshitaka Nagai
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-07-01
Series:Frontiers in Neurology
Subjects:
spinocerebellar ataxia type 8
repeat disease
parkinsonism
Canvas
RFC1
dysphagia
Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2025.1606305/full
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