P. GENÇPINAR Et Al. , "From Somatosensory Reflex Epilepsy to Dravet Syndrome Different Clinical Features due to novel SCN1A mutations of the p.Q422P amino acid," 14th International Child Neurology Congress , 2016
GENÇPINAR, P. Et Al. 2016. From Somatosensory Reflex Epilepsy to Dravet Syndrome Different Clinical Features due to novel SCN1A mutations of the p.Q422P amino acid. 14th International Child Neurology Congress .
GENÇPINAR, P., OLGAÇ DÜNDAR, N., ARICAN, P., ÇAVUŞOĞLU, D., ARSLAN, G., & İNCE, O. T., (2016). From Somatosensory Reflex Epilepsy to Dravet Syndrome Different Clinical Features due to novel SCN1A mutations of the p.Q422P amino acid . 14th International Child Neurology Congress
GENÇPINAR, PINAR Et Al. "From Somatosensory Reflex Epilepsy to Dravet Syndrome Different Clinical Features due to novel SCN1A mutations of the p.Q422P amino acid," 14th International Child Neurology Congress, 2016
GENÇPINAR, PINAR Et Al. "From Somatosensory Reflex Epilepsy to Dravet Syndrome Different Clinical Features due to novel SCN1A mutations of the p.Q422P amino acid." 14th International Child Neurology Congress , 2016
GENÇPINAR, P. Et Al. (2016) . "From Somatosensory Reflex Epilepsy to Dravet Syndrome Different Clinical Features due to novel SCN1A mutations of the p.Q422P amino acid." 14th International Child Neurology Congress .
@conferencepaper{conferencepaper, author={PINAR GENÇPINAR Et Al. }, title={From Somatosensory Reflex Epilepsy to Dravet Syndrome Different Clinical Features due to novel SCN1A mutations of the p.Q422P amino acid}, congress name={14th International Child Neurology Congress}, city={}, country={}, year={2016}}