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Spinocerebellar Ataxia 1 (SCA1)
Harry T. Orr
Laboratory Medicine and Pathology
Genetics Mechanisms of Cancer
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Keyphrases
Spinocerebellar Ataxia
100%
Ataxin-1
66%
Polyglutamine Tract
66%
Cognitive Deficits
33%
Neurodegenerative Diseases
33%
Motor Symptoms
33%
Huntington's Disease
33%
Autosomal Dominant
33%
Polyglutamine Disease
33%
Spinobulbar muscular Atrophy
33%
Dentatorubral-pallidoluysian Atrophy (DRPLA)
33%
Encoded Protein
33%
CAG Repeat
33%
Neuroscience
Polyglutamine
100%
Spinocerebellar Ataxia
100%
Ataxin 1
66%
Neurodegenerative Disorder
33%
Cognitive Disorders
33%
CAG Repeat
33%
Huntington's Disease
33%
Muscle Atrophy
33%
Dentatorubral-Pallidoluysian Atrophy
33%
Nucleus
33%