PRRT2 Mutations are the major cause of benign familial infantile seizures

PRRT2 Mutations are the major cause of benign familial infantile seizures is a paper indexed in ScholarIQ from OpenAlex.

How many citations does PRRT2 Mutations are the major cause of benign familial infantile seizures have?

PRRT2 Mutations are the major cause of benign familial infantile seizures has 107 citations in the OpenAlex counts ScholarIQ stores.

When was PRRT2 Mutations are the major cause of benign familial infantile seizures published?

PRRT2 Mutations are the major cause of benign familial infantile seizures has 2012 year in the ScholarIQ index.

What is the open-access status of PRRT2 Mutations are the major cause of benign familial infantile seizures?

PRRT2 Mutations are the major cause of benign familial infantile seizures has closed oa status in the ScholarIQ index.

What is the DOI of PRRT2 Mutations are the major cause of benign familial infantile seizures?

The DOI for PRRT2 Mutations are the major cause of benign familial infantile seizures is on the source record.

What is the PMID of PRRT2 Mutations are the major cause of benign familial infantile seizures?

The PMID for PRRT2 Mutations are the major cause of benign familial infantile seizures is on the source record.

What is the OpenAlex record for PRRT2 Mutations are the major cause of benign familial infantile seizures?

The OpenAlex for PRRT2 Mutations are the major cause of benign familial infantile seizures is on the source record.