Duran, G. S. Et Al. 2013. Severe scoliosis in a patient with COLQ mutation and congenital myasthenic syndrome: a clue for diagnosis. ACTA NEUROLOGICA BELGICA , vol.113, no.4 , 531-532.

Duran, G. S., Uzunhan, T. A., Ekici, B., Citak, A., Aydinli, N., & Caliskan, M., (2013). Severe scoliosis in a patient with COLQ mutation and congenital myasthenic syndrome: a clue for diagnosis. ACTA NEUROLOGICA BELGICA , vol.113, no.4, 531-532.

Duran, Guntulu Et Al. "Severe scoliosis in a patient with COLQ mutation and congenital myasthenic syndrome: a clue for diagnosis," ACTA NEUROLOGICA BELGICA , vol.113, no.4, 531-532, 2013

Duran, Guntulu S. Et Al. "Severe scoliosis in a patient with COLQ mutation and congenital myasthenic syndrome: a clue for diagnosis." ACTA NEUROLOGICA BELGICA , vol.113, no.4, pp.531-532, 2013

Duran, G. S. Et Al. (2013) . "Severe scoliosis in a patient with COLQ mutation and congenital myasthenic syndrome: a clue for diagnosis." ACTA NEUROLOGICA BELGICA , vol.113, no.4, pp.531-532.

@article{article, author={Guntulu Sare Duran 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={531-532} }