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Article

Late-onset episodic ataxia type 2 associated with a novel loss-of-function mutation in the CACNA1A gene

22 Feb 2009

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 19232643
DOI: 10.1016/j.jns.2009.01.005

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Related research

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Late-onset episodic ataxia type 2 associated with a novel loss-of-function mutation in the CACNA1A genePMID 19232643Read ↗

Identification of two novel mutations in the CACNA1A gene responsible for episodic ataxia type 2.Semantic proximity Read ↗

A Novel Frameshift CACNA1A Mutation Causing Episodic Ataxia Type 2.Semantic proximity Read ↗

Late-onset episodic ataxia type 2 due to an in-frame insertion in CACNA1A.Semantic proximity Read ↗

Early-Onset Cerebellar Atrophy Associated With Mutation in the CACNA1A GeneSemantic proximity Read ↗

A case of novel CACNA1A mutation causing type 2 episodic ataxia.Semantic proximity Read ↗

Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A geneSemantic proximity Read ↗

A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1Semantic proximity Read ↗

A novel CACNA1A mutation associated with adult-onset, paroxysmal head tremor.Semantic proximity Read ↗

Adult-onset ataxia or developmental disorder with seizures: two sides of missense changes in CACNA1A.Semantic proximity Read ↗

Three novel KCNA1 mutations in episodic ataxia type I familiesSemantic proximity Read ↗

Functional characterization of a novel mutation in KCNA1 in episodic ataxia type 1 associated with epilepsy.Semantic proximity Read ↗

Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia.Semantic proximity Read ↗

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