G. Gül Mert 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 , 529-534.
Gül Mert, G., Özcan, N., Herguner, O., Altunbaşak, Ş., İncecik, F., Bişgin, 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} }