The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy
The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy is a paper indexed in ScholarIQ from OpenAlex.
How many citations does The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy have?
The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy has 69 citations in the OpenAlex counts ScholarIQ stores.
When was The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy published?
The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy has 2012 year in the ScholarIQ index.
What is the open-access status of The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy?
The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy has bronze oa status in the ScholarIQ index.
What is the DOI of The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy?
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?
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?
The OpenAlex for The clinical utility of an <i>SCN1A</i> genetic diagnosis in infantile‐onset epilepsy is on the source record.