A case with Rett Syndrome caused by a novel mutation p.K298X in MECP2 gene

BAKIR A., ÇAVDARLI B.

12. Ulusal Tıbbi Genetik Kongresi, İzmir, Turkey, 05 October 2016, (Full Text)

  • Publication Type: Conference Paper / Full Text
  • City: İzmir
  • Country: Turkey
  • Ankara Yıldırım Beyazıt University Affiliated: Yes