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CLCN1
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CLCN1 Mutations in Czech Patients with Myotonia Congenita, In Silico Analysis of Novel and Known Mutations in the Human Dimeric Skeletal Muscle Chloride Channel
2013 |
Second Faculty of Medicine
publication
Rare variants in known and novel candidate genes predisposing to statin-associated myopathy
2016 |
Central Library of Charles University, First Faculty of Medicine