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Homozygosity for SCN4A Arg1142Gln causes congenital myopathy with variable disease expression

Christine K Sloth1, Federico Denti1, Nicole Schmitt1

  • 1Department of Neurology (C.K.S., D.G.), Odense University Hospital; and Department of Clinical Research (C.K.S., D.G.), Faculty of Health Sciences, University of Southern Denmark, Odense; Department of Biomedical Sciences (F.D., N.S., B.H.B.), Faculty of Health and Medical Sciences, University of Copenhagen; Department of Clinical Genetics (C.F.), Odense University Hospital; and Copenhagen Neuromuscular Center, Department of Neurology (J.V.), Rigshospitalet, University of Copenhagen, Denmark.

Neurology. Genetics
|October 5, 2018
PubMed
Abstract

No abstract available in PubMed .

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