Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleWhole exome sequencing identified a novel DAG1 mutation in a patient with rare, mild and late age of onset muscular dystrophy‐dystroglycanopathy.AuthorsDai, Yi; Liang, Shengran; Dong, Xue; Zhao, Yanhuan; Ren, Haitao; Guan, Yuzhou; Yin, Haifang; Li, Chen; Chen, Lin; Cui, Liying; Banerjee, SantasreePublicationJournal of Cellular & Molecular Medicine, 2019, Vol 23, Issue 2, p811ISSN1582-1838Publication typeArticleDOI10.1111/jcmm.13979