Related Experiment Video
Updated: May 16, 2026
09:34
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
A new SCARB2 mutation in a patient with progressive myoclonus ataxia without renal failure
Movement Disorders : Official Journal of the Movement Disorder Society
|December 11, 2012
Abstract
No abstract available in PubMed .
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