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

Linkage studies in alcohol-responsive myoclonic dystonia.

Movement disorders : official journal of the Movement Disorder Society - 1 Jul 1996

Gasser T, Bereznai B, Müller B, Pruszak-Seel R, Damrich R, Deuschl G, Oertel W H

Abstract excerpt

A large German family with "myoclonic dystonia with lightning jerks responsive to alcohol" was identified. Eleven affected pedigree members and six obligate gene carriers from five generations were identified. A description of one branch of this pedigree was published in 1964. Our examination 30 years after the initial report confirms the clinical syndrome of a nonprogressive movement disorder characterized by...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Aged
Share to Child

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Chromosome Aberrations

Share to Chromosome Mapping

Share to Genes, Dominant

Share to Genetic Linkage

Share to Genetic Markers

Source

Identifiers

PMID: 8813214
DOI: 10.1002/mds.870110403

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Linkage studies in alcohol-responsive myoclonic dystonia.PMID 8813214Read ↗

Genetics of primary dystonia.Semantic proximity Read ↗

Alcohol-responsive myoclonic dystonia in a large family: dominant inheritance and phenotypic variation.Semantic proximity Read ↗

Association of a missense change in the D2 dopamine receptor with myoclonus dystoniaSemantic proximity Read ↗

Inherited Myoclonus-dystonia syndrome: narrowing the 7q21-q31 locus in German families.Semantic proximity Read ↗

Molecular cloning and expression of rat torsinA in the normal and genetically dystonic (dt) rat.Semantic proximity Read ↗

Clinical and genetic evaluation of a family with a mixed dystonia phenotype from South Tyrol.Semantic proximity Read ↗

Candidate gene studies in focal dystonia.Semantic proximity Read ↗

Mutational and biochemical analysis of dopamine in dystonia: evidence for decreased dopamine D2 receptor inhibition.Semantic proximity Read ↗

Search for a founder mutation in idiopathic focal dystonia from Northern Germany.Semantic proximity Read ↗

Evaluation of the genes for the adrenergic receptors alpha 2A and alpha 1C and Gilles de la Tourette Syndrome.Semantic proximity Read ↗

A genetic study of idiopathic focal dystoniasSemantic proximity Read ↗

[Molecular-genetic analysis of torsion dystonia in Russia].Semantic proximity Read ↗

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