A clinical variant in SCN1A inherited from a mosaic fathercosegregates with a novel variant to cause Dravet syndrome in aconsanguineous family

TUNCER F. N., İŞCAN A., BAYKAL B., BEBEK N., ÇALIK M., UĞUR İŞERİ S. A., ...Daha Fazla

European Human Genetics Conference, 6 - 09 Haziran 2015

  • Yayın Türü: Bildiri
  • İstanbul Üniversitesi Adresli: Evet