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Article

Congenital mirror movements caused by a mutation in the DCC gene.

Developmental medicine and child neurology - 1 Aug 2015

Meneret Aurelie, Trouillard Oriane, Brochard Vanessa, Roze Emmanuel

Abstract excerpt

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Identifiers

PMID: 26011025
DOI: 10.1111/dmcn.12810

Genes

DCC

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

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Congenital mirror movements caused by a mutation in the DCC gene.PMID 26011025Read ↗

Mirror Hand Movements Caused by a Deletion of the DCC Gene.Semantic proximity Read ↗

A novel DCC mutation and genetic heterogeneity in congenital mirror movements.Semantic proximity Read ↗

Mutations in DCC Cause Congenital Mirror MovementsSemantic proximity Read ↗

Congenital mirror movements in a family: Outcomes associated with DCC mutations.Semantic proximity Read ↗

Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.Semantic proximity Read ↗

DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome.Semantic proximity Read ↗

Characterizing the phenotypes of congenital mirror movements and other rare genetic disorders.Semantic proximity Read ↗

Identification of a homozygous splice site mutation in the dynein axonemal light chain 4 gene on 22q13.1 in a large consanguineous family from Pakistan with congenital mirror movement disorder.Semantic proximity Read ↗

A human DCC variant causing mirror movement disorder reveals an essential role for the Wave regulatory complex in Netrin/DCC signalingSemantic proximity Read ↗

Neural function in DCC mutation carriers with and without mirror movementsSemantic proximity Read ↗

Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance.Semantic proximity Read ↗

Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected IndividualsSemantic proximity Read ↗

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