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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

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Identifiers

PMID: 25382112
DOI: 10.1002/mds.26066

Genes

GNAL

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Related research

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Research trail→

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

Screening of mutations in GNAL in sporadic dystonia patients.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 ↗

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

The genetics of dystonia: new twists in an old tale.Semantic proximity Read ↗

Pediatric Onset of Generalized Dystonia, Cognitive Impairment, and Dysmorphic Features in a Patient Carrying Compound Heterozygous GNAL Mutations.Semantic proximity Read ↗

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 ↗

Rare autosomal dominant mutations in GNAL are associated with primary torsion dystonia.Semantic proximity Read ↗

Genetics of dystonia: what's known? What's new? What's next?Semantic proximity Read ↗

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

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