Duran, G. Et Al. 2013. Severe scoliosis in a patient with COLQ mutation and congenital myasthenic syndrome: a clue for diagnosis.. Acta neurologica Belgica , vol.113 , 531-2.

Duran, G., Uzunhan, T., Ekici, B., Çıtak, A., Aydınlı, N., & Çalışkan, M., (2013). Severe scoliosis in a patient with COLQ mutation and congenital myasthenic syndrome: a clue for diagnosis.. Acta neurologica Belgica , vol.113, 531-2.

Duran, SARE Et Al. "Severe scoliosis in a patient with COLQ mutation and congenital myasthenic syndrome: a clue for diagnosis.," Acta neurologica Belgica , vol.113, 531-2, 2013

Duran, SARE G. Et Al. "Severe scoliosis in a patient with COLQ mutation and congenital myasthenic syndrome: a clue for diagnosis.." Acta neurologica Belgica , vol.113, pp.531-2, 2013

Duran, G. Et Al. (2013) . "Severe scoliosis in a patient with COLQ mutation and congenital myasthenic syndrome: a clue for diagnosis.." Acta neurologica Belgica , vol.113, pp.531-2.

@article{article, author={SARE GUNTULU SIK Et Al. }, title={Severe scoliosis in a patient with COLQ mutation and congenital myasthenic syndrome: a clue for diagnosis.}, journal={Acta neurologica Belgica}, year=2013, pages={531-2} }