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 (SCI-Expanded) identifier

  • Publication Type: Article / Abstract
  • Volume: 30 Issue: SUPPL 1
  • Publication Date: 2022
  • Journal Name: EUROPEAN JOURNAL OF HUMAN GENETICS
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, BIOSIS, CAB Abstracts, EMBASE, MEDLINE, Veterinary Science Database
  • Page Numbers: pp.255
  • Bursa Uludag University Affiliated: Yes