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Publications by Mark Tarnopolsky

Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia

American Journal of Human Genetics
Genetics
2019English

Anti-NT5c1A Autoantibodies as Biomarkers in Inclusion Body Myositis

Frontiers in Immunology
AllergyImmunology
2019English

Expanding Clinical Presentations Due to Variations in THOC2 mRNA Nuclear Export Factor

Frontiers in Molecular Neuroscience
Molecular NeuroscienceMolecular BiologyCellular
2020English

Mitochondrial Diseases in North America

Neurology: Genetics
NeurologyGenetics
2020English

Association of Common Variants in the Human Eyes Shut Ortholog (EYS) With Statin-Induced Myopathy: Evidence for Additional Functions of EYS

Muscle and Nerve
Molecular NeuroscienceNeurologyPhysiologyCellular
2011English

A Population-Based Study of Dystrophin Mutations in Canada

Canadian Journal of Neurological Sciences
MedicineNeurology
2011English

Corticotropin-Releasing Factor 2 Receptor Localization in Skeletal Muscle

Journal of Histochemistry and Cytochemistry
AnatomyHistology
2004English

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