Supplementary Tables - Polyglutamine Disorders

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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Additional Info

Field	Value
Theme
Author	Dilani Senthuran (12130773), William Schierding (1220838), Richard Roxburgh (1213425), Justin O'Sullivan (1198539)
Maintainer
Source	https://figshare.com/articles/dataset/Supplementary_Tables_-_Polyglutamine_Disorders/19228071
Source Created	2022-02-24T22:50:07Z
Source Modified	2022-02-24T22:50:07
Language	English
Spatial
Source Identifier	10.17608/k6.auckland.19228071.v1