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Nature Communications|November 24, 2020
SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial diseasePhilipp Gut, Sanna Matilainen, Jesse G Meyer, et al.
Cell Reports|July 3, 2026
Complex I drives glutamine-dependent TCA cycle to support viability of MYC<sup>high</sup> breast cancer cellsJohanna M Anttila, Mariel Savelius, Linda Id, et al.
American Journal of Human Genetics|April 2, 2021
Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genesCarolina Courage, Karen L Oliver, Eon Joo Park, et al.
Annals of Clinical and Translational Neurology|May 23, 2015
Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvementTobias B Haack, Christopher B Jackson, Kei Murayama, et al.
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