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Article

Association of CDH11 with non-syndromic ASD.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 1 Jul 2014

Crepel An, De Wolf Veerle, Brison Nathalie, Ceulemans Berten, Walleghem Didier, Peuteman Gilian, Lambrechts Diether, Steyaert Jean, Noens Ilse, Devriendt Koen, Peeters Hilde

Abstract excerpt

We report a sporadic patient with Autism Spectrum Disorder (ASD), mild intellectual disability and attention deficit hyperactivity disorder (ADHD) with a de novo partial deletion of CADHERIN 11 (CDH11). The deletion is associated with one of the breakpoints of a de novo complex chromosomal rearrangement 46,XY,t(3;16;5)(q29;q22;q15)inv4(p14;q21)ins(4;5)(q21;q14.3q15). Cadherins are cell adhesion molecules involved...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Child Development Disorders, Pervasive

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Source

Identifiers

PMID: 24839052
DOI: 10.1002/ajmg.b.32243

Genes

CDH11
CDH1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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