Early infantile epileptic encephalopathy (Ohtahara Syndrome): A case report with STXBP1 mutation

AYÇA S., Subay E. N.

17th International Child Neurology Congress, Antalya, Turkey, 03 October 2022, (Summary Text)

• Publication Type: Conference Paper / Summary Text
• City: Antalya
• Country: Turkey
• Manisa Celal Bayar University Affiliated: Yes