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Article

Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia.

Movement disorders : official journal of the Movement Disorder Society - 1 Mar 2012

Fogel Brent L, Lee Ji Yong, Lane Jessica, Wahnich Amanda, Chan Sandy, Huang Alden, Osborn Greg E, Klein Eric, Mamah Catherine, Perlman Susan, Geschwind Daniel H, Coppola Giovanni

Abstract excerpt

BACKGROUND: Sporadic-onset ataxia is common in a tertiary care setting but a significant percentage remains unidentified despite extensive evaluation. Rare genetic ataxias, reported only in specific populations or families, may contribute to a percentage of sporadic ataxia. METHODS: Patients with adult-onset sporadic ataxia, who tested negative for common genetic ataxias (SCA1, SCA2, SCA3, SCA6, SCA7, and/or...

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Source

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Identifiers

PMID: 22287014
DOI: 10.1002/mds.24064
PMCID: PMC3323119

Genes

LMNB1
PDYN
SACS
SETX
TGM6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

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