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Sachdev, E., Tabatabai, R., Roy, V., Rimel, B

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3.2.3.1 15q11-q13 The most common deletion/duplication syndrome associated with ASD phenotypes is the duplication syndrome of chromosome 15q11-q13.This region not only harbors the coding genes for GABA-A receptor 3 (GABRB3), 5 (GABRA5), and 3 (GABRG3) subunits but also serves as a genetic vulnerability hotspot due to its enrichment in low-copy repeats (LCRs)Deletions in the BP1-BP3 breakpoint regions are associated with ASD syndromes (64, 65)

A meta-analysis evaluated iodine supplementation during pregnancy in areas with mild-to-moderate iodine deficiency

doi: 10.3389/fcell.2022.841831 Received 22 December 2021 Accepted 09 February 2022 Published 11 March 2022 Volume 10 - 2022 Edited by Chisa Shukunami, Hiroshima University, Japan Reviewed by Petra Kraus, Clarkson University, United States Danny Chan, The University of Hong Kong, Hong Kong SAR, China Updates Copyright 2022 Hickman, Rathan-Kumar and Peck