Oculopharyngodistal myopathy is a distinct entity: clinical and genetic features of 47 patients

Durmus H, Laval SH, Deymeer F, Parman Y, Kiyan E, Gokyigiti M, Ertekin C, Ercan I, Solakoglu S, Karcagi V, Straub V, Bushby K, Lochm?oller H, Serdaroglu-Oflazer P. Oculopharyngodistal myopathy is a distinct entity: clinical and genetic features of 47 patients. Neurology. 2011 Jan 18;76(3):227-35.

PubMed ID: 
21242490