Associated Papers
Mitochondrial CHCHD2: Disease-Associated Mutations, Physiological Functions, and Current Animal Models.
Kee TR et al.
Frontiers in Aging Neuroscience, 2021
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy.
Lin CH et al.
Brain : a Journal of Neurology, 2020
33141179 (PubMed )
Supplement: awaa279_supplementary_data.zip › awaa279-suppl_data › brain-2020-00357-File010.pdf
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