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Genetic Modifiers of Hereditary Neuromuscular Disorders and Cardiomyopathy.
Cells
February 2021
Heart, Lung and Vascular Institute, Division of Cardiovascular Health and Disease, Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA.
Novel genetic variants exist in patients with hereditary neuromuscular disorders (NMD), including muscular dystrophy. These patients also develop cardiac manifestations. However, the association between these gene variants and cardiac abnormalities is understudied.
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First Department of Neurology, Eginition Hospital, Medical School, National and Kapodistrian University of Athens, Greece.
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Department of Neurology, School of Medicine, Fukushima Medical University.
[Valosin-containing protein-related amyotrophic lateral sclerosis in Japan].
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April 2016
Department of Neurology, Kindai University Sakai Hospital.
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Planta
April 2001
Department of Plant Biology, University of Illinois, Urbana, IL 61801, USA.
Calmodulin (CaM), a primary Ca2+ receptor in all eukaryotic cells, is a multifunctional protein that functions by interacting with and modulating the activities of a wide variety of target proteins. Identifying and characterizing these CaM-binding target proteins is essential to define the pathways by which Ca(2+)-regulated signals are transduced. An Arabidopsis thaliana L.
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