Durmuş, H. Et Al. 2011. Oculopharyngodistal myopathy is a distinct entity Clinical and genetic features of 47 patients. NEUROLOGY , vol.76, no.3 , 227-235.

Durmuş, H., LAVAL, S. H., Deymeer, F., Parman, Y., Kiyan, E., GOKYIGITI, M., ... Ertekin, C.(2011). Oculopharyngodistal myopathy is a distinct entity Clinical and genetic features of 47 patients. NEUROLOGY , vol.76, no.3, 227-235.

Durmuş, Hacer Et Al. "Oculopharyngodistal myopathy is a distinct entity Clinical and genetic features of 47 patients," NEUROLOGY , vol.76, no.3, 227-235, 2011

Durmuş, Hacer Et Al. "Oculopharyngodistal myopathy is a distinct entity Clinical and genetic features of 47 patients." NEUROLOGY , vol.76, no.3, pp.227-235, 2011

Durmuş, H. Et Al. (2011) . "Oculopharyngodistal myopathy is a distinct entity Clinical and genetic features of 47 patients." NEUROLOGY , vol.76, no.3, pp.227-235.

@article{article, author={Hacer Durmuş Et Al. }, title={Oculopharyngodistal myopathy is a distinct entity Clinical and genetic features of 47 patients}, journal={NEUROLOGY}, year=2011, pages={227-235} }