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Article

Rare autosomal dominant mutations in GNAL are associated with primary torsion dystonia.

Clinical genetics - 1 Sept 2013

Kaur A

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Topics

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Share to Dystonia Musculorum Deformans
Share to GTP-Binding Protein alpha Subunits
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Source

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

Identifiers

PMID: 23621094
DOI: 10.1111/cge.12178

Genes

GNAL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 25 Oct 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

Rare autosomal dominant mutations in GNAL are associated with primary torsion dystonia.PMID 23621094Read ↗

Genetic and clinical features of primary torsion dystonia.Semantic proximity Read ↗

Genetics of primary torsion dystonia.Semantic proximity Read ↗

Novel GNAL mutations in two German patients with sporadic dystonia.Semantic proximity Read ↗

[Primary torsion dystonia--clinical and molecular aspects].Semantic proximity Read ↗

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

Update on the genetics of primary torsion dystonia loci DYT6, DYT7, and DYT13 and the dystonia-plus locus DYT12.Semantic proximity Read ↗

Mutations in GNAL cause primary torsion dystonia.Semantic proximity Read ↗

Clinical presentation and progression of sporadic and familial primary torsion dystonia in Italy.Semantic proximity Read ↗

Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystoniaSemantic proximity Read ↗

Clinical and molecular genetics of primary dystonias.Semantic proximity Read ↗

Novel GNAL mutation with intra-familial clinical heterogeneity: Expanding the phenotype.Semantic proximity Read ↗

De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient.Semantic proximity Read ↗

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