K. AYDIN Et Al. , "A New Homozygous Mutatıon On Npc2 Gene: As A Cause Of Refractory Epılepsy In A Child.," 12th European Congress on Epileptology Prague, Czech Republic 11th - 15th September, 2016 , 2016
AYDIN, K. Et Al. 2016. A New Homozygous Mutatıon On Npc2 Gene: As A Cause Of Refractory Epılepsy In A Child.. 12th European Congress on Epileptology Prague, Czech Republic 11th - 15th September, 2016 .
AYDIN, K., TEKİN ORGUN, L., ARHAN, E., AKBAŞ, Y., & SERDAROĞLU, A., (2016). A New Homozygous Mutatıon On Npc2 Gene: As A Cause Of Refractory Epılepsy In A Child. . 12th European Congress on Epileptology Prague, Czech Republic 11th - 15th September, 2016
AYDIN, KÜRŞAD Et Al. "A New Homozygous Mutatıon On Npc2 Gene: As A Cause Of Refractory Epılepsy In A Child.," 12th European Congress on Epileptology Prague, Czech Republic 11th - 15th September, 2016, 2016
AYDIN, KÜRŞAD Et Al. "A New Homozygous Mutatıon On Npc2 Gene: As A Cause Of Refractory Epılepsy In A Child.." 12th European Congress on Epileptology Prague, Czech Republic 11th - 15th September, 2016 , 2016
AYDIN, K. Et Al. (2016) . "A New Homozygous Mutatıon On Npc2 Gene: As A Cause Of Refractory Epılepsy In A Child.." 12th European Congress on Epileptology Prague, Czech Republic 11th - 15th September, 2016 .
@conferencepaper{conferencepaper, author={KÜRŞAD AYDIN Et Al. }, title={A New Homozygous Mutatıon On Npc2 Gene: As A Cause Of Refractory Epılepsy In A Child.}, congress name={12th European Congress on Epileptology Prague, Czech Republic 11th - 15th September, 2016}, city={}, country={}, year={2016}}