The X-linked dystonia-parkinsonism syndrome (XDP): clinical and molecular genetic analysis.

doi:10.1111/j.1750-3639.1992.tb00706.x

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

Back to search

Article

The X-linked dystonia-parkinsonism syndrome (XDP): clinical and molecular genetic analysis.

Brain pathology (Zurich, Switzerland) - 1 Oct 1992

Graeber M B, Müller U

Abstract excerpt

Dystonia and parkinsonism are two major representatives of movement disorders. The X-linked dystonia-parkinsonism syndrome (XDP) serves as a model system for the study of both dystonia and parkinsonism since both symptom complexes occur together and are inherited as Mendelian traits with very high penetrance. XDP, which is endemic to the Philippine island of Panay, originated by a single mutation ("genetic...

Topics

Base Sequence
Chromosome Mapping
Chromosomes, Artificial, Yeast
Cloning, Molecular
DNA
Dystonia Musculorum Deformans
Female
Gene Library
Genetic Linkage
Humans
Lod Score
Male

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Parkinson Disease, Secondary

Pedigree

Phenotype

Polymorphism, Restriction Fragment Length

Recombination, Genetic

X Chromosome

Source

Open in PubMed

Identifiers

PMID: 1364136
DOI: 10.1111/j.1750-3639.1992.tb00706.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-1364136-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The X-linked dystonia-parkinsonism syndrome (XDP): clinical and molecular genetic analysis.PMID 1364136Read ↗

New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3).Semantic proximity Read ↗

Sex linked recessive dystonia parkinsonism of Panay, Philippines (XDP).Semantic proximity Read ↗

X-linked recessive dystonia parkinsonism (XDP; Lubag; DYT3).Semantic proximity Read ↗

The phenotype of the X-linked dystonia-parkinsonism syndrome. An assessment of 42 cases in the Philippines.Semantic proximity Read ↗

X-linked dystonia parkinsonism syndrome (XDP, lubag): disease-specific sequence change DSC3 in TAF1/DYT3 affects genes in vesicular transport and dopamine metabolismSemantic proximity Read ↗

Specific sequence changes in multiple transcript system DYT3 are associated with X-linked dystonia parkinsonism.Semantic proximity Read ↗

DXS106 and DXS559 flank the X-linked dystonia-parkinsonism syndrome locus (DYT3).Semantic proximity Read ↗

Phenotypic and molecular analyses of X-linked dystonia-parkinsonism ("lubag") in women.Semantic proximity Read ↗

The unique phenomenology of sex-linked dystonia parkinsonism (XDP, DYT3, "Lubag").Semantic proximity Read ↗

The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene.Semantic proximity Read ↗

Phenomenology of "Lubag" or X-linked dystonia-parkinsonism.Semantic proximity Read ↗

Rapid-onset dystonia-parkinsonism: Linkage to chromosome 19q13Semantic proximity Read ↗

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