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Article

Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene

3 Dec 2005

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 16325861
DOI: 10.1016/j.jns.2005.10.007

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Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A genePMID 16325861Read ↗

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

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

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Adult-onset ataxia or developmental disorder with seizures: two sides of missense changes in CACNA1A.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 CACNA1A mutation associated with adult-onset, paroxysmal head tremor.Semantic proximity Read ↗

Identification of a novel mutation in the CACNA1C gene in a Chinese family with autosomal dominant cerebellar ataxiaSemantic proximity Read ↗

Episodic ataxia type 2: phenotype characteristics of a novel CACNA1A mutation and review of the literature.Semantic proximity Read ↗

Rare CACNA1A mutations leading to congenital ataxia.Semantic proximity Read ↗

CACNA1A Mutations Causing Early Onset Ataxia: Profiling Clinical, Dysmorphic and Structural-Functional Findings.Semantic proximity Read ↗

Infantile-Onset Syndromic Cerebellar Ataxia and CACNA1G MutationsSemantic proximity Read ↗

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