Article
SMN promotes mitochondrial metabolic maturation during myogenesis by regulating the MYOD-miRNA axis
2022-02-14
Abstract excerpt
Spinal muscular atrophy (SMA) is a congenital neuromuscular disease caused by the mutation or deletion of survival motor neuron 1 ( SMN1 ) gene. Although the primary cause of progressive muscle atrophy in SMA has classically been considered the degeneration of motor neurons, recent studies have indicated a skeletal muscle-specific pathological phenotype such as impaired mitochondrial function and enhanced cell d...
Topics
Open a Topic to create a Post that cites this publication.
Identifiers and source
- Literature Corpus work
- cee1fcbd-2613-5fcf-a70c-64db174c8d49
- DOI
- 10.1101/2022.02.13.480288
