GÜL MERT, G. Et Al. 2021. Congenital myasthenic syndrome in Turkey: clinical and genetic features in the long-term follow-up of patients. Acta Neurologica Belgica , vol.121, no.2 , 529-534.

GÜL MERT, G., ÖZCAN, N., Hergüner, Ö., ALTUNBAŞAK, Ş., İNCECİK, F., BİŞGİN, A., ... CEYLANER, S.(2021). Congenital myasthenic syndrome in Turkey: clinical and genetic features in the long-term follow-up of patients. Acta Neurologica Belgica , vol.121, no.2, 529-534.

GÜL MERT, GÜLEN Et Al. "Congenital myasthenic syndrome in Turkey: clinical and genetic features in the long-term follow-up of patients," Acta Neurologica Belgica , vol.121, no.2, 529-534, 2021

GÜL MERT, GÜLEN G. Et Al. "Congenital myasthenic syndrome in Turkey: clinical and genetic features in the long-term follow-up of patients." Acta Neurologica Belgica , vol.121, no.2, pp.529-534, 2021

GÜL MERT, G. Et Al. (2021) . "Congenital myasthenic syndrome in Turkey: clinical and genetic features in the long-term follow-up of patients." Acta Neurologica Belgica , vol.121, no.2, pp.529-534.

@article{article, author={GÜLEN GÜL MERT Et Al. }, title={Congenital myasthenic syndrome in Turkey: clinical and genetic features in the long-term follow-up of patients}, journal={Acta Neurologica Belgica}, year=2021, pages={529-534} }