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Updated: Sep 22, 2025

Author Spotlight: Decoding Mitochondrial Aging
Published on: June 30, 2023
Cutting the Gordian Knot of a Mitochondrial Disease
1Montreal Neurological Institute, McGill University, Montreal, QC, Canada; Department of Human Genetics, McGill University, Montreal, QC, Canada.
Abstract:
The advent of whole-exome sequencing ushered in a new era of in the genetic diagnosis of rare diseases, but characterizing large alterations in genome architecture has remained challenging. In this issue of Med, Frazier et al. harnessed the power of genomics and proteomics to identify a recurrent duplication as the molecular basis of a fatal perinatal mitochondrial cardiomyopathy.1.
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