• 0 Citations
  • 0 h-Index
If you made any changes in Pure, your changes will be visible here soon.

Fingerprint Dive into the research topics where Meagan Hainlen is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

Mitochondrial Dynamics Medicine & Life Sciences
Muscular Dystrophies Medicine & Life Sciences
Mitochondrial DNA Medicine & Life Sciences
Mutation Medicine & Life Sciences
Fibroblasts Medicine & Life Sciences
Mitochondrial Proteins Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Mitochondrial Diseases Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 2019 2019

MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement

Care4Rare Canada Consortium, Dec 1 2019, In : Acta Neuropathologica. 138, 6, p. 1013-1031 19 p.

Research output: Contribution to journalArticle

Mitochondrial Dynamics
Muscular Dystrophies
Mitochondrial DNA