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Article

A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1

25 Sept 2008

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Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 18926884
DOI: 10.1016/j.neuroscience.2008.09.022

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Related research

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Research trail→

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A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1PMID 18926884Read ↗

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 ↗

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

Two novel KCNA1 variants identified in two unrelated Chinese families affected by episodic ataxia type 1 and neurodevelopmental disorders.Semantic proximity Read ↗

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

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

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

A novel mutation in KCNA1 causes episodic ataxia without myokymiaSemantic proximity Read ↗

Novel mutation in KCNA1 causes episodic ataxia with paroxysmal dyspnea.Semantic proximity Read ↗

A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctionsSemantic proximity Read ↗

Genetic Variants Associated with Episodic Ataxia in Korea.Semantic proximity Read ↗

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

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