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Spinocerebellar Ataxia 1 (SCA1)
Harry T. Orr
Laboratory Medicine and Pathology
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Medicine & Life Sciences
Spinocerebellar Ataxias
100%
polyglutamine
97%
Ataxin-1
86%
X-Linked Bulbo-Spinal Atrophy
38%
Huntington Disease
27%
Atrophy
21%
Neurodegenerative Diseases
21%
Proteins
9%
Chemical Compounds
Disorder
63%
Protein
30%