Hyaline inclusion myopathy: Unmasked by statin therapy
Author:
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/mus.21079/fullpdf
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4. Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy;Bohlega;Neurology,2004
5. Motor unit territory in different human muscles;Buchthal;Acta Physiol Scand,1959
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1. Role of genetics in the prediction of statin-associated muscle symptoms and optimization of statin use and adherence;Cardiovascular Research;2018-06-05
2. Myosin storage myopathy mutations yield defective myosin filament assembly in vitro and disrupted myofibrillar structure and function in vivo;Human Molecular Genetics;2017-09-14
3. Genetics of Muscle Disease;Muscle Disease;2013-07-08
4. Genetics of neuromuscular disorders;Critical Reviews in Clinical Laboratory Sciences;2012-04
5. Drug-related Myopathies of Which the Clinician Should Be Aware;Current Rheumatology Reports;2010-04-27
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