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The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy

PaperCitations, authors & open-access status

The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy is a paper indexed in PICO Portal from OpenAlex.

How many citations does The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy have?

PICO Portalcitation count

The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy has 69 citations in the OpenAlex counts PICO Portal stores.

When was The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy published?

PICO Portalyear

The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy has 2012 year in the PICO Portal index.

What is the open-access status of The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy?

PICO Portaloa status

The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy has bronze oa status in the PICO Portal index.

What is the DOI of The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy?

PICO Portaldoi

The DOI for The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy is on the source record.

What is the PMID of The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy?

PICO Portalpmid

The PMID for The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy is on the source record.

What is the OpenAlex record for The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy?

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The OpenAlex for The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy is on the source record.

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