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Article

Novel GNAL mutations in two German patients with sporadic dystonia.

Movement disorders : official journal of the Movement Disorder Society - 1 Dec 2014

Ziegan Julia, Wittstock Matthias, Westenberger Ana, Dobričić Valerija, Wolters Alexander, Benecke Reiner, Klein Christine, Kamm Christoph

Abstract excerpt

No abstract is available from the source.

Topics

Dystonic Disorders
GTP-Binding Protein alpha Subunits
Genetic Predisposition to Disease
Germany
Humans
Mutation

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 25382112
DOI: 10.1002/mds.26066

Genes

GNAL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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Novel GNAL mutations in two German patients with sporadic dystonia.PMID 25382112Read ↗

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

A new mutation in the GNAL gene in familial dystonia presenting with mental symptoms.Semantic proximity Read ↗

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Recent genetic advances in early-onset dystonia.Semantic proximity Read ↗

Genetic Dystonias: Update on Classification and New Genetic Discoveries.Semantic proximity Read ↗

Update on the Genetics of Dystonia.Semantic proximity Read ↗

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Movement disorders in 2014. Genetic advances spark a revolution in dystonia phenotyping.Semantic proximity Read ↗

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