HuGE Literature Finder
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PRRT2 mutations: exploring the phenotypical boundaries. Journal of neurology, neurosurgery, and psychiatry 2014 Apr 85 (4): 462-5. Djémié Tania, Weckhuysen Sarah, Holmgren Philip, Hardies Katia, Van Dyck Tine, Hendrickx Rik, Schoonjans An-Sofie, Van Paesschen Wim, Jansen Anna C, De Meirleir Linda, Selim Laila Abdel Moteleb, Girgis Marian Y, Buyse Gunnar, Lagae Lieven, Smets Katrien, Smouts Iris, Claeys Kristl G, Van den Bergh Vic, Grisar Thierry, Blatt Ilan, Shorer Zamir, Roelens Filip, Afawi Zaid, Helbig Ingo, Ceulemans Berten, De Jonghe Peter, Suls Arv |
Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes. Genes, brain, and behavior 2013 Mar 12 (2): 234-40. Liu X-R, Wu M, He N, Meng H, Wen L, Wang J-L, Zhang M-P, Li W-B, Mao X, Qin J-M, Li B-M, Tang B, Deng Y-H, Shi Y-W, Su T, Yi Y-H, Tang B-S, Liao W |
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