Spinocerebellar ataxia with ocular motor apraxia and DNA repair

Neuropathology

Volumn 26, Issue 4, 2006, Pages 361-367

  Onodera, Osamu ^a  

^a NIIGATA UNIVERSITY   (Japan)

Author keywords

Aprataxin; Ataxia; Early onset ataxia with ocular motor apraxia and hypoalbuminemia ataxia; Ocular motor apraxia; Oculomotor apraxia type 1; Single strand break repair

Indexed keywords

APRATAXIN; DNA; DOUBLE STRANDED DNA; MYELIN; PROTEIN; RNA; SINGLE STRANDED DNA; UNCLASSIFIED DRUG;

APRAXIA; ATAXIA TELANGIECTASIA; ATAXIA WITH OCULOMOTOR APRAXIA 1; CELL LOSS; CONFERENCE PAPER; DISEASE ASSOCIATION; DISEASE SEVERITY; DNA REPAIR; DNA REPLICATION; DNA STRAND BREAKAGE; EARLY ONSET ATAXIA WITH OCULAR MOTOR APRAXIA AND HYPOALBUMINEMIA; GENE FUNCTION; HUMAN; HYPOALBUMINEMIA; MOTOR NEUROPATHY; NERVE CELL; NERVE DEGENERATION; NYSTAGMUS; OCULAR MOTOR APRAXIA; OCULOMOTOR NERVE DISEASE; PERIPHERAL NEUROPATHY; PRIORITY JOURNAL; PROTEIN FUNCTION; PURKINJE CELL; SENSORY NEUROPATHY; SPINOCEREBELLAR DEGENERATION;

ANIMALS; APRAXIAS; DNA REPAIR; DNA-BINDING PROTEINS; HUMANS; HYPOALBUMINEMIA; NERVE DEGENERATION; NUCLEAR PROTEINS; OCULAR MOTILITY DISORDERS; SPINOCEREBELLAR ATAXIAS;

EID: 33746164726     PISSN: 09196544     EISSN: 14401789     Source Type: Journal    
DOI: 10.1111/j.1440-1789.2006.00741.x     Document Type: Conference Paper

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