Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleClinical phenotype of autosomal dominant progressive external ophthalmoplegia in a family with a novel mutation in the C10orf2 gene.AuthorsHong D; Bi H; Yao S; Wang Z; Yuan Y; Hong, Daojun; Bi, Hongyan; Yao, Sheng; Wang, Zhaoxia; Yuan, YunPublicationMuscle & Nerve, 2010, Vol 41, Issue 1, p92ISSN0148-639XPublication typejournal articleDOI10.1002/mus.21439