Novel mouse models of oculopharyngeal muscular dystrophy (OPMD) reveal early onset mitochondrial defects and suggest loss of PABPN1 may contribute to pathology
Katherine E. Vest; Brittany L. Phillips; Ayan Banerjee; Luciano H. Apponi; Eric B. Dammer; Weiting Xu; Dinghai Zheng; Julia Yu; Bin Tian; Grace K. Pavlath; Anita H. Corbett
Author Information: Department of Pharmacology, Emory University School of Medicine, Atlanta, GA, USA
|Checking for direct PDF access through Ovid|
Abstract unavailable for this article.