TY  - GEN
AU  - Robitaille,Y
AU  - Schut,L
AU  - Kish,S J
TI  - Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype
SN  - 0001-6322
PY  - 1996///0605
KW  - Adolescent
KW  - Adult
KW  - Atrophy
KW  - Brain
KW  - pathology
KW  - Child
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 6
KW  - ultrastructure
KW  - Dentate Gyrus
KW  - Humans
KW  - Immunohistochemistry
KW  - Middle Aged
KW  - Mutation
KW  - Neural Pathways
KW  - Olivopontocerebellar Atrophies
KW  - genetics
KW  - Phenotype
KW  - Red Nucleus
KW  - Spinal Cord
KW  - Spinocerebellar Degenerations
N1  - Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1007/BF00318569
ER  -