The complex clinical and genetic classification of inherited ataxias. II. Autosomal recessive ataxias

Neurological Sciences

Volumn 22, Issue 3, 2001, Pages 219-228

  Di Donato, S ^a   Gellera, C ^a   Mariotti, C ^a  

^a DEPARTMENT OF NEUROSURGERY   (Italy)

Author keywords

Abetalipoproteinemia; Ataxia telangiectasia; Ataxia with oculomotor apraxia; Autosomal recessive cerebellar ataxia; Friedreich's ataxia; Refsum's disease; Spinocerebellar ataxia; Vitamin E deficiency

Indexed keywords

ALPHA TOCOPHEROL; CELL PROTEIN; DNA;

ABETALIPOPROTEINEMIA; ALPHA TOCOPHEROL DEFICIENCY; APRAXIA; ATAXIA TELANGIECTASIA; AUTOSOMAL RECESSIVE DISORDER; CELL CYCLE; CEREBELLAR ATAXIA; CLINICAL FEATURE; DEGENERATIVE DISEASE; DIFFERENTIAL DIAGNOSIS; DISEASE CLASSIFICATION; DNA METABOLISM; DNA REPAIR; EUROPE; EYE DISEASE; FRIEDREICH ATAXIA; GENETIC COUNSELING; GENETICS; HOMEOSTASIS; HUMAN; METABOLISM; NEUROLOGIC DISEASE; PATHOGENESIS; PROGNOSIS; REVIEW; SPINOCEREBELLAR DEGENERATION;

ATAXIA TELANGIECTASIA; FRIEDREICH ATAXIA; GENES, RECESSIVE; HUMANS; SPINOCEREBELLAR ATAXIAS;

EID: 0035178023     PISSN: 15901874     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100720100017     Document Type: Review

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