From Somatosensory Reflex Epilepsy to Dravet Syndrome Different Clinical Features due to novel SCN1A mutations of the p.Q422P amino acid

GENÇPINAR P., OLGAÇ DÜNDAR N., ARICAN P., ÇAVUŞOĞLU D., ARSLAN G., İNCE O. T.

14th International Child Neurology Congress, 1 - 05 May 2016, (Summary Text)

• Publication Type: Conference Paper / Summary Text
• Dokuz Eylül University Affiliated: Yes