PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome
scientific article published on January 2012
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author: Jozef Gécz, Hadassa Goldberg-Stern, Sarah E Heron, Eric Herlenius, Ingrid Scheffer, Samuel Berkovic, Amos D. Korczyn, Sameer M Zuberi, Lynette Sadleir, Leanne Dibbens, James Pelekanos, Bronwyn E Grinton, Sara Kivity, Zaid Afawi
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