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Supplementary Tables - Polyglutamine Disorders

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posted on 2022-02-24, 22:50 authored by Dilani Senthuran, William SchierdingWilliam Schierding, Richard RoxburghRichard Roxburgh, Justin O'SullivanJustin O'Sullivan
Supplementary Tables supporting the spatial constraint analysis (CoDeS3D) of Polyglutamine Disorder-related genetic markers regulating 9 diseases.

Diseases: Spinocerebellar Ataxia 1 (SCA 1), Spinocerebellar Ataxia 2 (SCA 2), Spinocerebellar Ataxia 3 (SCA 3), Spinocerebellar Ataxia 6 (SCA 6), Spinocerebellar Ataxia 7 (SCA 7), Spinocerebellar Ataxia 17 (SCA 17), Dentatorubropallidoluysian Atrophy (DRPLA), Spinal Bulbar Muscular Atrophy (SBMA) and Huntington’s Disease (HD)

Genes: ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7, TBP, ATN1, AR, HTT

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