Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleStart codon mutation of GYG1 causing late-onset polyglucosan body myopathy with nemaline rods.AuthorsTasca, Giorgio; Fattori, Fabiana; Monforte, Mauro; Hedberg-Oldfors, Carola; Sabatelli, Mario; Udd, Bjarne; Boldrini, Renata; Bertini, Enrico; Ricci, Enzo; Oldfors, AndersAbstractA letter to the editor is presented regarding a case study of an 84-years-old male who was diagnosed with glycogen storage disease type XV, a form of polyglucosan body myopathy.SubjectsGLYCOGEN storage disease; DIAGNOSIS of muscle diseasesPublicationJournal of Neurology, 2016, Vol 263, Issue 10, p2133ISSN0340-5354Publication typeLetterDOI10.1007/s00415-016-8268-z