Association of a Novel<i>ACTA1</i>Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended Family
Kristen Zukosky(National Institutes of Health), Carsten G. Bönnemann(National Institute of Neurological Disorders and Stroke), James J. Collins(Broad Institute), Ozge Ceyhan‐Birsoy(Memorial Sloan Kettering Cancer Center), Toby A. Ferguson(UK Dementia Research Institute), Līvija Medne(Children's Hospital of Philadelphia), Bryan J. Traynor(National Institutes of Health), Jahannaz Dastgir(National Institute of Neurological Disorders and Stroke), Yaqun Zou(National Institutes of Health), Michele Yang(Children's Hospital Colorado), Markus Meier(University of Manitoba), Alan H. Beggs(Boston Children's Hospital), Katherine G. Meilleur(National Institutes of Health), Kevin J. Felice(Hospital for Special Care), Marcella Devoto(Children's Hospital of Philadelphia), Jörg Stetefeld(University of Manitoba), Lauren Elman(University of Pennsylvania), Richard S. Finkel(St. Jude Children's Research Hospital), Jachinta Rooney(National Institutes of Health), Janel O. Johnson(National Institutes of Health), J. Raphael Gibbs(National Institutes of Health), Gihan Tennekoon(Children's Hospital of Philadelphia), Joachim Schessl(Ludwig-Maximilians-Universität München)
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