Determination of genetic changes in etiology of autism spectrum disorder in twins by whole-exome sequencing

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dc.contributor.authorHayretdag, Ceyda
dc.contributor.authorAlgedik, Pinar
dc.contributor.authorEkmekci, Cumhur Gokhan
dc.contributor.authorGunal, Ozlem Bozdagi
dc.contributor.authorAgyuz, Umut
dc.contributor.authorYildirim, Halime
dc.contributor.authorCoskunpinar, Ender
dc.date.accessioned2025-10-16T15:21:23Z
dc.date.issued2020
dc.identifier.doi10.1016/j.genrep.2020.100618
dc.identifier.otherWOS:000550665700033
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/7661
dc.publisherELSEVIER
dc.sourceGENE REPORTS
dc.subjectAutism spectrum disorders
dc.subjectGenetic mutation
dc.subjectMonozygotic
dc.subjectWhole exome sequencing
dc.subjectFMN2
dc.subjectKCNQ2
dc.subjectNOTCH3
dc.subjectTMRC6A
dc.subjectSHANK3
dc.subjectSLC6A4
dc.titleDetermination of genetic changes in etiology of autism spectrum disorder in twins by whole-exome sequencing
dc.typeArticle

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