Loss of CHCHD2 and CHCHD10 activates OMA1 peptidase to disrupt mitochondrial cristae phenocopying patient mutations
Dominant mutations in the mitochondrial paralogs coiled-helix-coiled-helix (CHCHD) domain 2 (C2) and CHCHD10 (C10) were recently identified as causing Parkinson's disease and amyotrophic lateral sclerosis/frontotemporal dementia/myopathy, respectively. The mechanism by which they disrupt mitoch...
Main Authors: | Liu, Y-T, Huang, X, Nguyen, D, Shammas, MK, Wu, BP, Dombi, E, Springer, DA, Poulton, J, Sekine, S, Narendra, DP |
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Format: | Journal article |
Language: | English |
Published: |
Oxford University Press
2020
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