Neuromuscular transmission deficits in patients with CMT and ClC‐1 inhibition in CMT animal models

Abstract Objective Charcot–Marie Tooth (CMT) is a hereditary neuropathy characterized by muscle weakness and fatigue with no approved therapies. Preclinical studies implicate neuromuscular junction (NMJ) transmission deficits in muscle dysfunction in CMT. This study aimed to evaluate NMJ function in...

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Hlavní autoři:	Thomas Skjærlund Grønnebæk, Helga Haahr‐Lillevang, Martin Skov, Kristina Kelly, Nathan R. Kerr, Jose A. Viteri, Andrea Jaworek, Amy Bartlett, Jane Bold, John Hutchison, Jorge Quiroz, Hatice Tankisi, Thomas Holm Pedersen, Henning Andersen, William David Arnold
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Wiley 2025-02-01
Edice:	Annals of Clinical and Translational Neurology
On-line přístup:	https://doi.org/10.1002/acn3.52252
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