Robitaille, Y <br/><br/>
Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype.  [electronic resource] 

 -  Acta neuropathologica  1995 
 - 572-81 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0001-6322 
<br/><br/><label>Standard No.: </label>10.1007/BF00318569  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Atrophy<br/>Brain--pathology<br/>Child<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 6--ultrastructure<br/>Dentate Gyrus--pathology<br/>Humans<br/>Immunohistochemistry<br/>Middle Aged<br/>Mutation<br/>Neural Pathways--pathology<br/>Olivopontocerebellar Atrophies--genetics<br/>Phenotype<br/>Red Nucleus--pathology<br/>Spinal Cord--pathology<br/>Spinocerebellar Degenerations--genetics