Determination of genetic changes in etiology of autism spectrum disorder in twins by whole-exome sequencing - Hayretdag, Ceyda; Algedik, Pinar; Ekmekci, Cumhur Gokhan; Gunal, Ozlem Bozdagi; Agyuz, Umut; Yildirim, Halime; Coskunpinar, Ender (ELSEVIER, 2020)
Keywords: Autism spectrum disorders; Genetic mutation; Monozygotic; Whole exome sequencing; FMN2; KCNQ2; NOTCH3; TMRC6A; SHANK3; SLC6A4