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A Wide Spectrum of Genetic Disorders Causing Severe Childhood Epilepsy in Taiwan: A Case Series of Ultrarare Genetic Cause and Novel Mutation Analysis in a Pilot Study

PaperCitations, authors & open-access status

A Wide Spectrum of Genetic Disorders Causing Severe Childhood Epilepsy in Taiwan: A Case Series of Ultrarare Genetic Cause and Novel Mutation Analysis in a Pilot Study is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 27 citations, 2020 year and gold oa status.

27
Citations
2020
Year
gold
OA Status

Related on ScholarIQ

Syuan‐Yu Hong
Author
Journal of Personalized Medicine
Journal
Genomics and Rare Diseases
Topic
Genomics and Rare Diseases
Topic
Epilepsy research and treatment
Topic
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Topic
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