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disease > genetic disease > hereditary disease > dentatorubropallidoluysian atrophy
disease > degenerative disease > dentatorubropallidoluysian atrophy
... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > epilepsy > dentatorubropallidoluysian atrophy

Término preferido

dentatorubropallidoluysian atrophy  

Definición

  • Dentatorubral–pallidoluysian atrophy (DRPLA) is an autosomal dominant spinocerebellar degeneration caused by an expansion of a CAG repeat encoding a polyglutamine tract in the atrophin-1 protein. (Wikipedia)

Concepto genérico

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URI

http://data.loterre.fr/ark:/67375/VH8-RRMB4HWN-T

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