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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.- Sort by
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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 Thomas
Research output: Contribution to journal › Article › peer-review