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bn:00908964n
Noun Concept
JA
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
病気
希少疾患
脊髄小脳変性症
EN
Huntington's disease-like syndrome
GENETIC ASSOCIATION
EN
ATN1
HEALTH SPECIALTY
神経学

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