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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 24, 2012
Deletion of exon 26 of the dystrophin gene is associated with a mild Becker muscular dystrophy phenotypeNanna Witting, Morten Duno, John VissingFrontiers in Genetics|November 2, 2020
Mutation Load of Single, Large-Scale Deletions of mtDNA in Mitotic and Postmitotic TissuesTina D Jeppesen, Morten Duno, John VissingNeurology|July 13, 2006
Autosomal dominant monosymptomatic myotonia permanensEskild Colding-Jørgensen, Morten Duno, John VissingAnnals of Human Genetics|May 28, 2009
High-resolution melting facilitates mutation screening of PYGM in patients with McArdle diseaseMorten Duno, Ros Quinlivan, John Vissing, et al.JAMA Neurology|November 13, 2013
Severe axial myopathy in McArdle diseaseNanna Witting, Morten Duno, Monique Piraud, et al.Neurology. Genetics|March 31, 2017
Phenotypes, genotypes, and prevalence of congenital myopathies older than 5 years in DenmarkNanna Witting, Ulla Werlauff, Morten Duno, et al.Muscle & Nerve|July 15, 2015
Prevalence and phenotypes of congenital myopathy due to α-actin 1 gene mutationsNanna Witting, Ulla Werlauff, Morten Duno, et al.Brain : a Journal of Neurology|May 13, 2009
Splice mutations preserve myophosphorylase activity that ameliorates the phenotype in McArdle diseaseJohn Vissing, Morten Duno, Marianne Schwartz, et al.European Journal of Human Genetics : EJHG|March 14, 2008
cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in DenmarkMorten Duno, Marie-Louise Sveen, Marianne Schwartz, et al.Muscle & Nerve|February 10, 2015
LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophiesNicoline Løkken, Alfred Peter Born, Morten Duno, et al.Pageof 45