Scholar IQ
Try ScholarIQ free
Upload Records Snowball Search Search OpenAlex
About the database
ScholarIQanswers from OpenAlex

Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions

PaperCitations, authors & open-access status

Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 267 citations, 2012 year and gold oa status.

267
Citations
2012
Year
gold
OA Status

Related on ScholarIQ

Betül Baykan
Author
Roberto Caraballo
Author
Genomics and Rare Diseases
Topic
Genomics and Rare Diseases
Topic
Genetics and Neurodevelopmental Disorders
Topic
Epilepsy research and treatment
Topic
470M+ articles · free account