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2. Mutation analysis of PRRT2 in two Chinese BFIS families and nomenclature of PRRT2 related paroxysmal diseases. Wang JL; Mao X; Hu ZM; Li JD; Li N; Guo JF; Jiang H; Shen L; Li J; Shi YT; Xia K; Liu JY; Liao WP; Tang BS Neurosci Lett; 2013 Sep; 552():40-5. PubMed ID: 23896529 [TBL] [Abstract][Full Text] [Related]
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7. [Clinical features and PRRT2 mutations in infantile convulsions with paroxysmal choreoathetosis]. Yang X; Zhang Y; Xu X; Wang S; Yang Z; Wu Y; Zhang X; Liu X; Wu X Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):679-85. PubMed ID: 25449067 [TBL] [Abstract][Full Text] [Related]
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