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5. Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis. Yang X; Zhang Y; Xu X; Wang S; Yang Z; Wu Y; Liu X; Wu X BMC Neurol; 2013 Dec; 13():209. PubMed ID: 24370076 [TBL] [Abstract][Full Text] [Related]
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