Publications by authors named "Ori Rokach"

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Epigenetic changes as a common trigger of muscle weakness in congenital myopathies.
Ori Rokach, Marijana Sekulic-Jablanovic, Nicol Voermans, Jo Wilmshurst, Komala Pillay

Hum Mol Genet· August 2015

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Variable myopathic presentation in a single family with novel skeletal RYR1 mutation.
Ruben Attali, Sharon Aharoni, Susan Treves, Ori Rokach, Michal Becker Cohen

PLoS One· February 2014

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Establishment of a human skeletal muscle-derived cell line: biochemical, cellular and electrophysiological characterization.
Ori Rokach, Nina D Ullrich, Martin Rausch, Vincent Mouly, Haiyan Zhou

Biochem J· October 2013

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RyR1 deficiency in congenital myopathies disrupts excitation-contraction coupling.
Haiyan Zhou, Ori Rokach, Lucy Feng, Iulia Munteanu, Kamel Mamchaoui

Hum Mutat· July 2013

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