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bn:00908964n
Noun Concept
SYL
No term available
EN
Dentatorubral–pallidoluysian atrophy is an autosomal dominant spinocerebellar degeneration caused by an expansion of a CAG repeat encoding a polyglutamine tract in the atrophin-1 protein. Wikipedia
Relations
Sources
IS A
EN
disease
EN
rare disease
EN
spinocerebellar ataxia
EN
Huntington's disease-like syndrome
GENETIC ASSOCIATION
EN
ATN1
HEALTH SPECIALTY
EN
neurology

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