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De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy
PaperCitations, authors & open-access status
De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 1,289 citations, 2001 year and bronze oa status.
1,289
Citations
2001
Year
bronze
OA Status