Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype

Acta Neuropathologica

Volumn 90, Issue 6, 1995, Pages 572-581

  Robitaille, Yves ^a,b   Schut, Lawrence ^c   Kish, Stephen J ^d  

^a UNIVERSITÉ DE MONTRÉAL   (Canada)

^b UNIVERSITY OF MONTREAL   (Canada)

^c UNIVERSITY OF MINNESOTA   (United States)

^d CENTRE FOR ADDICTION AND MENTAL HEALTH   (Canada)

Author keywords

Ataxia; Dentatorubral atrophy; Olivopontocerebellar atrophy; Spinocerebellar ataxia type 1

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CEREBELLAR ATAXIA; CHROMOSOME 12; CHROMOSOME 14; CLINICAL ARTICLE; CRANIAL NERVE; GENE MUTATION; HUMAN; HUMAN TISSUE; IMMUNOCYTOCHEMISTRY; IMMUNOREACTIVITY; LOCUS CERULEUS; MOTONEURON; NERVE CELL DEGENERATION; NEUROANATOMY; NEUROPATHOLOGY; OLIVOPONTOCEREBELLAR ATROPHY; PRIORITY JOURNAL; PURKINJE CELL; SCHOOL CHILD; SPINAL CORD;

ADOLESCENT; ADULT; ATROPHY; BRAIN; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 6; DENTATE GYRUS; HUMAN; IMMUNOHISTOCHEMISTRY; MIDDLE AGE; MUTATION; NEURAL PATHWAYS; OLIVOPONTOCEREBELLAR ATROPHIES; PHENOTYPE; RED NUCLEUS; SPINAL CORD; SPINOCEREBELLAR DEGENERATIONS; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0028832215     PISSN: 00016322     EISSN: 14320533     Source Type: Journal    
DOI: 10.1007/BF00318569     Document Type: Article

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