Hereditary disorders of the nervous system from anatomo-clinical studies to molecular biology

Acta Neurologica Belgica

Volumn 96, Issue 3, 1996, Pages 240-246

  Martin, J J ^a  

^a UNIVERSITY OF ANTWERP   (Belgium)

Author keywords

Alzheimer's disease; Heredity; Molecular biology; Nervous system; Peripheral neuropathies; Spinocerebellar degenerations

Indexed keywords

ALZHEIMER DISEASE; ARTICLE; CEREBELLAR ATAXIA; CHROMOSOME 17; GENETIC PROCEDURES; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; OLIVOPONTOCEREBELLAR ATROPHY; PHENOTYPE; POINT MUTATION; SPINOCEREBELLAR DEGENERATION;

ALZHEIMER DISEASE; CEREBELLAR ATAXIA; CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOMES, HUMAN, PAIR 17; GENETIC TECHNIQUES; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMANS; OLIVOPONTOCEREBELLAR ATROPHIES; PHENOTYPE; POINT MUTATION; SPINOCEREBELLAR DEGENERATIONS;

EID: 0030238858     PISSN: 03009009     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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