CHCHD2 and Parkinson's disease
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology
Reference1 articles.
1. CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study;Funayama;Lancet Neurol,2015
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1. Parkinson’s Disease is Predominantly a Genetic Disease;Journal of Parkinson's Disease;2024-04-23
2. Genetic and pharmacologic p32-inhibition rescue CHCHD2-linked Parkinson’s disease phenotypes in vivo and in cell models;Journal of Biomedical Science;2024-02-23
3. Neurodegeneration-associated mitochondrial proteins, CHCHD2 and CHCHD10–what distinguishes the two?;Frontiers in Cell and Developmental Biology;2022-09-09
4. CHCHD2 and CHCHD10: Future therapeutic targets in cognitive disorder and motor neuron disorder;Frontiers in Neuroscience;2022-08-18
5. Mitochondrial CHCHD2: Disease-Associated Mutations, Physiological Functions, and Current Animal Models;Frontiers in Aging Neuroscience;2021-04-22
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