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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.

Muscular Dystrophies Medicine & Life Sciences
Mitochondrial DNA Medicine & Life Sciences
Mitochondrial Dynamics 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

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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

Muscular Dystrophies
Mitochondrial DNA
Mitochondrial Dynamics