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

Search for a founder mutation in idiopathic focal dystonia from Northern Germany.

American journal of human genetics - 1 Dec 1998

Klein C, Ozelius L J, Hagenah J, Breakefield X O, Risch N J, Vieregge P

Abstract excerpt

Both the discovery of the DYT1 gene on chromosome 9q34 in autosomal dominant early-onset torsion dystonia and the detection of linkage for one form of adult-onset focal dystonia to chromosome 18p (DYT7) in a family from northern Germany provide the opportunity to further investigate genetic factors in the focal dystonias. Additionally, reports of linkage disequilibrium between several chromosome 18 markers and...

Read the complete abstract on PubMed

Topics

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

Share to Age of Onset
Share to Aged
Share to Alleles

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

Share to Carrier Proteins

Share to Gene Frequency

Share to Germany

Share to Heterozygote

Share to Linkage Disequilibrium

Source

Open in PubMed Open full text

Identifiers

PMID: 9837831
DOI: 10.1086/302143
PMCID: PMC1377650

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Search for a founder mutation in idiopathic focal dystonia from Northern Germany.PMID 9837831Read ↗

Sporadic focal dystonia in northwest Germany: molecular basis on chromosome 18p.Semantic proximity Read ↗

Evidence for DYT7 being a common cause of cervical dystonia (torticollis) in Central Europe.Semantic proximity Read ↗

The role of DYT1 in primary torsion dystonia in Europe.Semantic proximity Read ↗

DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13–36.32 in an Italian family with cranial‐cervical or upper limb onsetSemantic proximity Read ↗

Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant inheritance and purely focal distributionSemantic proximity Read ↗

A novel locus for autosomal recessive primary torsion dystonia (DYT17) maps to 20p11.22–q13.12Semantic proximity Read ↗

Primary torsion dystonia: the search for genes is not overSemantic proximity Read ↗

Identification of a novel primary torsion dystonia locus (DYT13) on chromosome 1p36 in an Italian family with cranial-cervical or upper limb onset.Semantic proximity Read ↗

Is TOR1A a risk factor in adult-onset primary torsion dystonia?Semantic proximity Read ↗

DYT1 mutations amongst early onset primary dystonia patients in China.Semantic proximity Read ↗

Unbalanced whole arm translocation resulting in loss of 18p in dystoniaSemantic proximity Read ↗

Non-DYT1 early-onset primary torsion dystonia: comparison with DYT1 phenotype and review of the literature.Semantic proximity Read ↗

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