Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder.

doi:10.1038/s41598-017-12317-3

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Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder.

Scientific reports - 21 Sept 2017

Hnoonual Areerat, Thammachote Weerin, Tim-Aroon Thipwimol, Rojnueangnit Kitiwan, Hansakunachai Tippawan, Sombuntham Tasanawat, Roongpraiwan Rawiwan, Worachotekamjorn Juthamas, Chuthapisith Jariya, Fucharoen Suthat, Wattanasirichaigoon Duangrurdee, Ruangdaraganon Nichara, Limprasert Pornprot, Jinawath Natini

Abstract excerpt

Chromosomal microarray (CMA) is now recognized as the first-tier genetic test for detection of copy number variations (CNVs) in patients with autism spectrum disorder (ASD). The aims of this study were to identify known and novel ASD associated-CNVs and to evaluate the diagnostic yield of CMA in Thai patients with ASD. The Infinium CytoSNP-850K BeadChip was used to detect CNVs in 114 Thai patients comprised of 68...

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PMID: 28935972
DOI: 10.1038/s41598-017-12317-3
PMCID: PMC5608768

Genes

SERINC2

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