Characterizing a de novo TRIO gene variant as a likely cause of autosomal dominant Intellectual developmental disorder type 63 with macrocephaly


Tekguc D. C. , Tuncel G., Karanlik S., Koreken N., TEMEL Ş. G. , Ergoren M. C.

EUROPEAN JOURNAL OF HUMAN GENETICS, vol.30, no.SUPPL 1, pp.255, 2022 (Journal Indexed in SCI) identifier

  • Publication Type: Article / Abstract
  • Volume: 30 Issue: SUPPL 1
  • Publication Date: 2022
  • Title of Journal : EUROPEAN JOURNAL OF HUMAN GENETICS
  • Page Numbers: pp.255