[K08] Role of Proteasome Overload in Pathogenesis of Retinitis Pigmentosa

Ente: National Eye Institute

Scadenza: 2027-04-30

Importo max: $170,704

Paese: US

Descrizione

PROJECT SUMMARY / ABSTRACT Retinitis pigmentosa (RP) is the most common hereditary cause of blindness, affecting over 1.5 million people worldwide. RP has an extraordinarily variable etiology, with over 5,000 distinct mutations in more than 300 genes implicated in its pathogenesis, which suggests t

Settori: National Eye Institute

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