Determination of genetic changes in etiology of autism spectrum disorder in twins by whole-exome sequencing
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Date
Journal Title
Journal ISSN
Volume Title
dc.identifier.issn
dc.identifier.doi
10.1016/j.genrep.2020.100618
dc.identifier.other
WOS:000550665700033
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dc.description.issue
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ELSEVIER
DOI
10.1016/j.genrep.2020.100618
Abstract
Description
Keywords
Autism spectrum disorders , Genetic mutation , Monozygotic , Whole exome sequencing , FMN2 , KCNQ2 , NOTCH3 , TMRC6A , SHANK3 , SLC6A4