Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders.

J Neurodev Disord · 2023 · PMC10148449 · PMID 37120522

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Cases with ADHD In ADHD cases but not ASD cases, we found deletions significantly enriched at 5 CNVRs-5q32 ( ADRB2, SH3TC2 ), 10q26.11 ( PRLHR ), 1q25.1 ( CACYBP ), 7p22.1 ( FSCN1 ), 18q21.32 (MC4R), although there is a trend toward significance at the FSCN1 locus for individuals with both ASD and ADHD.

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