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Progression of biological markers in spinocerebellar ataxia type 3: analysis of longitudinal data from the ESMI cohort

2025-01-31

Abstract excerpt

<h4>Background</h4> Spinocerebellar ataxia type 3 (SCA3) is an autosomal dominantly inherited adult-onset disease. We aimed to describe longitudinal changes in clinical and biological findings and to identify predictors for clinical progression. <h4>Methods</h4> We used data from participants enrolled in the ESMI cohort collected between Nov 09, 2016 and July 18, 2023. The data freeze included data from 14 sites i...

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Literature Corpus work
41e58b5b-80dc-567f-b5bb-86f545a1db3c
DOI
10.1101/2025.01.30.25321426
Open publication

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Progression of biological markers in spinocerebellar ataxia type 3: analysis of longitudinal data from the ESMI cohortDOI 10.1101/2025.01.30.25321426
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