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Updated: Aug 8, 2026

A Simple Composite Phenotype Scoring System for Evaluating Mouse Models of Cerebellar Ataxia
07:33

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Published on: May 21, 2010

Case Report of Myoclonus-Ataxia Syndrome in an Indian Patient Due to SCNA1 Gene Mutation

Anjali Chouksey1

  • 1Neurology Consultant, Department of Neurology, Gastro-Neuro Clinic, Jabalpur, India.

Movement Disorders Clinical Practice
|March 29, 2025
PubMed
Abstract

No abstract available in PubMed .

Keywords:
Dravet syndromeSCNA1 mutationmyoclonus‐ataxia syndrome

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