The clinical features and classification of the late onset autosomal dominant cerebellar ataxias: A STUDY of 11 families, INCLUDING descendants OF 'the DREW family OF walworth'

Brain

Volumn 105, Issue 1, 1982, Pages 1-28

  Harding, A E ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ATAXIA; AUTOSOMAL DOMINANT INHERITANCE; CENTRAL NERVOUS SYSTEM; CEREBELLAR ATAXIA; CLASSIFICATION; HEREDITY; MAJOR CLINICAL STUDY; ONSET AGE; PEDIGREE;

ADULT; AGED; ATROPHY; BASAL GANGLIA DISEASES; CEREBELLAR ATAXIA; CEREBELLUM; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; DEMENTIA; FEMALE; GENES, DOMINANT; HUMAN; MALE; MIDDLE AGE; NERVE DEGENERATION; OLIVARY NUCLEUS; OPHTHALMOPLEGIA; OPTIC ATROPHY; PEDIGREE; PONS; SPINAL CORD; SUPPORT, NON-U.S. GOV'T;

EID: 0019902437     PISSN: 00068950     EISSN: None     Source Type: Journal    
DOI: 10.1093/brain/105.1.1     Document Type: Article

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