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Article

A subgroup of spinocerebellar ataxias defective in DNA damage responses.

Neuroscience - 14 Apr 2007

Gueven N, Chen P, Nakamura J, Becherel O J, Kijas A W, Grattan-Smith P, Lavin M F

Abstract excerpt

A subgroup of human autosomal recessive ataxias is also characterized by disturbances of eye movement or oculomotor apraxia. These include ataxia telangiectasia (A-T); ataxia telangiectasia like disorder (ATLD); ataxia oculomotor apraxia type 1 (AOA1) and ataxia oculomotor apraxia type 2 (AOA2). What appears to be emerging is that all of these have in common some form of defect in DNA damage response which could...

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Identifiers

PMID: 17224243
DOI: 10.1016/j.neuroscience.2006.12.010

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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