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Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects

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Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects is a paper indexed in PICO Portal from OpenAlex.

How many citations does Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects have?

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Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects has 81 citations in the OpenAlex counts PICO Portal stores.

When was Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects published?

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Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects has 2020 year in the PICO Portal index.

What is the open-access status of Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects?

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Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects has bronze oa status in the PICO Portal index.

What is the DOI of Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects?

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The OpenAlex for Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects is on the source record.

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