Gencpinar, P. Et Al. 2019. Clinical and Molecular Manifestations of Congenital Muscular Alpha-Dystroglycanopathy due to an ISPD Gene Mutation. NEUROPHYSIOLOGY , vol.51, no.5 , 373-378.

Gencpinar, P., Uyanik, G., Haspolat, S., Oygur, N., & Duman, O., (2019). Clinical and Molecular Manifestations of Congenital Muscular Alpha-Dystroglycanopathy due to an ISPD Gene Mutation. NEUROPHYSIOLOGY , vol.51, no.5, 373-378.

Gencpinar, P. Et Al. "Clinical and Molecular Manifestations of Congenital Muscular Alpha-Dystroglycanopathy due to an ISPD Gene Mutation," NEUROPHYSIOLOGY , vol.51, no.5, 373-378, 2019

Gencpinar, P. Et Al. "Clinical and Molecular Manifestations of Congenital Muscular Alpha-Dystroglycanopathy due to an ISPD Gene Mutation." NEUROPHYSIOLOGY , vol.51, no.5, pp.373-378, 2019

Gencpinar, P. Et Al. (2019) . "Clinical and Molecular Manifestations of Congenital Muscular Alpha-Dystroglycanopathy due to an ISPD Gene Mutation." NEUROPHYSIOLOGY , vol.51, no.5, pp.373-378.

@article{article, author={P. Gencpinar Et Al. }, title={Clinical and Molecular Manifestations of Congenital Muscular Alpha-Dystroglycanopathy due to an ISPD Gene Mutation}, journal={NEUROPHYSIOLOGY}, year=2019, pages={373-378} }