Biblio
Absence of full-length dystrophin impairs normal maturation and contraction of cardiomyocytes derived from human induced pluripotent stem cells. Cardiovasc Res. 2019.
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Gene Therapy for Inherited Muscle Diseases: Where Genetics Meets Rehabilitation Medicine. Am J Phys Med Rehabil. 2014;93(11 Suppl 3):S97-S107.
. Gene therapy in monogenic congenital myopathies. Methods. 2015.
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Incomplete-penetrant hypertrophic cardiomyopathy G256E mutation causes hypercontractility and elevated mitochondrial respiration. Proc Natl Acad Sci U S A. 2024;121(19):e2318413121.
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