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Mitochondrial Dysfunction and Stress Responses in CHCHD10 Myopathy and Neurodegeneration

Shammas, MarioUniversity of Cambridge2023

… dominant mutations in the mitochondrial protein CHCHD10 and its paralogue CHCHD2 were shown to cause familial amyotrophic lateral sclerosis and Parkinson’s disease, respectively, with phenotypes that often resemble the idiopathic forms of the diseases. Different mutations in CHCHD10 cause …

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