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

Myoclonus-dystonia (DYT11) with novel SGCE mutation misdiagnosed as a primary psychiatric disorder.

Journal of the neurological sciences - 15 Nov 2014

Bonello M, Larner A J, Alusi S H

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Anxiety Disorders
Share to Diagnostic Errors
Share to Dystonic Disorders
Share to SGCE gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Sarcoglycans

Source

Identifiers

PMID: 25204586
DOI: 10.1016/j.jns.2014.08.043

Genes

SGCE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Myoclonus-dystonia (DYT11) with novel SGCE mutation misdiagnosed as a primary psychiatric disorder.PMID 25204586Read ↗

Hereditary myoclonus dystonia (DYT11): a novel SGCE gene mutation with intrafamilial phenotypic heterogeneity.Semantic proximity Read ↗

Myoclonus-dystonia: detection of novel, recurrent, and de novo SGCE mutations.Semantic proximity Read ↗

Hereditary Myoclonus Dystonia: A Novel SGCE Variant and Phenotype Including Intellectual Disability.Semantic proximity Read ↗

Novel SGCE gene mutation in a Korean patient with myoclonus-dystonia with unique phenotype mimicking Moya-Moya disease.Semantic proximity Read ↗

Novel and de novo mutations of the SGCE gene in Brazilian patients with myoclonus-dystonia.Semantic proximity Read ↗

A mixed-ethnicity myoclonus-dystonia patient with a novel SGCE nonsense mutation: a case report.Semantic proximity Read ↗

A novel mutation of the SGCE-gene in a German family with myoclonus-dystonia syndrome.Semantic proximity Read ↗

Heterozygous YY1 mutation - A mimicker of SGCE-myoclonus-dystonia.Semantic proximity Read ↗

Myoclonus-dystonia syndrome.Semantic proximity Read ↗

SGCE Myoclonus-Dystonia: An Inherited Movement Disorder.Semantic proximity Read ↗

A novel SGCE variant is associated with myoclonus-dystonia with phenotypic variability.Semantic proximity Read ↗

Childhood-Onset Myoclonus-Dystonia Due to KCTD17 Mutation: A Case Report and Review of Diagnostic Challenges.Semantic proximity Read ↗

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