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Publications by Alan H. Beggs

Mutations of Tropomyosin 3 (TPM3) Are Common and Associated With Type 1 Myofiber Hypotrophy in Congenital Fiber Type Disproportion

Human Mutation
Genetics
2010English

Aberrant Regulation of Epigenetic Modifiers Contributes to the Pathogenesis in Patients With Selenoprotein N ‐ Related Myopathies

Human Mutation
Genetics
2019English

Treatment With ActRIIB-mFc Produces Myofiber Growth and Improves Lifespan in the Acta1 H40Y Murine Model of Nemaline Myopathy

American Journal of Pathology
Forensic MedicinePathology
2016English

Clinical Heterogeneity Associated With KCNA1 Mutations Include Cataplexy and Nonataxic Presentations

Neurogenetics
Molecular NeuroscienceGeneticsCellular
2015English

Muscle Dysfunction in a Zebrafish Model of Duchenne Muscular Dystrophy

Physiological Genomics
GeneticsPhysiology
2016English

Development of Soft Tissue Sarcomas in Ribosomal Proteins L5 and S24 Heterozygous Mice

Journal of Cancer
Oncology
2016English

ACTN3 Genotype Is Associated With Human Elite Athletic Performance

American Journal of Human Genetics
Genetics
2003English

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