De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood is a paper indexed in ScholarIQ from OpenAlex.

How many citations does De novo mutations in ATP1A3 cause alternating hemiplegia of childhood have?

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood has 425 citations in the OpenAlex counts ScholarIQ stores.

When was De novo mutations in ATP1A3 cause alternating hemiplegia of childhood published?

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood has 2012 year in the ScholarIQ index.

What is the open-access status of De novo mutations in ATP1A3 cause alternating hemiplegia of childhood?

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood has green oa status in the ScholarIQ index.

What is the DOI of De novo mutations in ATP1A3 cause alternating hemiplegia of childhood?

The DOI for De novo mutations in ATP1A3 cause alternating hemiplegia of childhood is on the source record.

What is the PMID of De novo mutations in ATP1A3 cause alternating hemiplegia of childhood?

The PMID for De novo mutations in ATP1A3 cause alternating hemiplegia of childhood is on the source record.

What is the OpenAlex record for De novo mutations in ATP1A3 cause alternating hemiplegia of childhood?

The OpenAlex for De novo mutations in ATP1A3 cause alternating hemiplegia of childhood is on the source record.