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Journal of Neurology, Neurosurgery, and Psychiatry|June 17, 2009
New aspects on patients affected by dysferlin deficient muscular dystrophyLars Klinge, Ahmed Aboumousa, Michelle Eagle, et al.
Journal of Cell Science|January 21, 2017
Dysferlin mediates membrane tubulation and links T-tubule biogenesis to muscular dystrophyJulia Hofhuis, Kristina Bersch, Ronja Büssenschütt, et al.
Human Molecular Genetics|March 17, 2009
Attenuated muscle regeneration is a key factor in dysferlin-deficient muscular dystrophyYen-Hui Chiu, Mark A Hornsey, Lars Klinge, et al.
Muscle & Nerve|January 19, 2010
Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscleLars Klinge, John Harris, Caroline Sewry, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|June 24, 2020
Dysferlin links excitation-contraction coupling to structure and maintenance of the cardiac transverse-axial tubule systemJulia Hofhuis, Kristina Bersch, Stefan Wagner, et al.
Human Molecular Genetics|August 27, 2015
Muscle weakness in TPM3-myopathy is due to reduced Ca2+-sensitivity and impaired acto-myosin cross-bridge cycling in slow fibresMichaela Yuen, Sandra T Cooper, Steve B Marston, et al.
Circulation Research|January 2, 2010
A common MLP (muscle LIM protein) variant is associated with cardiomyopathyRalph Knöll, Sawa Kostin, Stefanie Klede, et al.
Human Mutation|April 3, 2014
Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathiesMinttu Marttila, Vilma-Lotta Lehtokari, Steven Marston, et al.
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