Title : Molecular Mechanisms and Therapeutics for Spinocerebellar Ataxia Type 2.

Pub. Date : 2019 Oct

PMID : 31435879






3 Functional Relationships(s)
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1 The effective therapeutic treatment and the disease-modifying therapy for spinocerebellar ataxia type 2 (SCA2) (a progressive hereditary disease caused by an expansion of polyglutamine in the ataxin-2 protein) is not available yet. polyglutamine ataxin 2 Homo sapiens
2 The effective therapeutic treatment and the disease-modifying therapy for spinocerebellar ataxia type 2 (SCA2) (a progressive hereditary disease caused by an expansion of polyglutamine in the ataxin-2 protein) is not available yet. polyglutamine ataxin 2 Homo sapiens
3 The effective therapeutic treatment and the disease-modifying therapy for spinocerebellar ataxia type 2 (SCA2) (a progressive hereditary disease caused by an expansion of polyglutamine in the ataxin-2 protein) is not available yet. polyglutamine ataxin 2 Homo sapiens