Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Congenital mirror movements: phenotypes associated with DCC and RAD51 mutations.

Journal of the neurological sciences - 15 Apr 2015

Franz Elizabeth A, Chiaroni-Clarke Rachel, Woodrow Stephanie, Glendining Kelly A, Jasoni Christine L, Robertson Stephen P, Gardner R J McKinlay, Markie David

Abstract excerpt

Congenital mirror movements (CMM) is a disorder characterized by unintentional mirroring in homologous motor systems of voluntary movements on the opposite side, usually affecting the distal upper extremities. Genetic analyses have revealed involvement of three genes (DCC, RAD51, and DNAL4). We sought to distinguish whether different phenotypes of CMM exist, and if so, whether they might map to different...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Axonemal Dyneins
Share to DCC Receptor

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Movement Disorders

Share to Pedigree

Share to Rad51 Recombinase

Share to Receptors, Cell Surface

Share to Tumor Suppressor Proteins

Share to Young Adult

Source

Identifiers

PMID: 25813273
DOI: 10.1016/j.jns.2015.03.006

Genes

DCC
RAD51
DNAL4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Congenital mirror movements: phenotypes associated with DCC and RAD51 mutations.PMID 25813273Read ↗

Congenital mirror movements are associated with defective polymerisation of RAD51.Semantic proximity Read ↗

RAD51 haploinsufficiency causes congenital mirror movements in humans.Semantic proximity Read ↗

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

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

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

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

Mutations in DCC Cause Congenital Mirror MovementsSemantic proximity Read ↗

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

Congenital mirror movements caused by a mutation in the DCC gene.Semantic proximity Read ↗

Congenital Mirror Movements in A Family with TUBB2B Mutation.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 ↗

⌁Select a neighboring publication to make it the new centre.