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	1.	[Clinical and genetic diagnosis of Dravet syndrome: report of 20 cases]. [electronic resource] by Siegler, Zsuzsa Neuwirth, Magdolna Hegyi, Márta Paraicz, Eva Pálmafy, Beatrix Tegzes, Andrea Barsi, Péter Karcagi, Veronika Claes, Lieve De Jonghe, Peter Herczegfalvi, Agnes Fogarasi, András Producer: 20081231 In: Ideggyogyaszati szemle vol. 61 Availability: No items available. Save to lists Add to cart (remove)
	2.	The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene. [electronic resource] by Gempel, Klaus Topaloglu, Haluk Talim, Beril Schneiderat, Peter Schoser, Benedikt G H Hans, Volkmar H Pálmafy, Beatrix Kale, Gulsev Tokatli, Aysegul Quinzii, Catarina Hirano, Michio Naini, Ali DiMauro, Salvatore Prokisch, Holger Lochmüller, Hanns Horvath, Rita Producer: 20070906 In: Brain : a journal of neurology vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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