PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome

Sarah Heron, Bronwyn Grinton, Sara Kivity, Zaid Afawi, Sameer Zuberi, James Hughes, Claire Pridmore, Bree Hodgson, Xenia Iona, Lynette Sadleir, James Pelekanos, Eric Herlenius, Hadassa Goldberg-Stern, Haim Bassan, Eric Haan, Amos Korczyn, Alison Gardner, Mark Corbett, Jozef Gecz, Paul ThomasJC Mulley, Samuel Berkovic, Ingrid Scheffer, Leanne Dibbens

    Research output: Contribution to journalArticlepeer-review

    231 Citations (Scopus)

    Fingerprint

    Dive into the research topics of 'PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome'. Together they form a unique fingerprint.

    Medicine and Dentistry

    Neuroscience