De novo GABRB3 c.103G>A mutation detected in a patient with epilepsy and speech retardation


AKBAŞ N. E., SÖNMEZ V., AKCAN M. B., MUTLUER Y. E., CELİK K. M., SILAN F., ...More

6. Uluslararası Katılımlı Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Turkey, 16 September 2021, (Summary Text)

  • Publication Type: Conference Paper / Summary Text
  • City: Kayseri
  • Country: Turkey
  • Çanakkale Onsekiz Mart University Affiliated: Yes