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Prevalence and phenotypes of congenital myopathy due to α‐actin 1 gene mutations
Authors:Nanna Witting MD  PhD  Ulla Werlauff PhD  Morten Duno PhD  John Vissing MD  DMSc
Affiliation:1. Copenhagen Neuromuscular Center, Department of Neurology, Copenhagen, Denmark;2. Danish National Rehabilitation Center for Neuromuscular Diseases, Aarhus, Denmark;3. Department of Clinical Genetics, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
Abstract:
Keywords:ACTA1  congenital myopathy  nemaline myopathy  phenotype  prevalence
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