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	1.	Infantile and pediatric quinone deficiency diseases. [electronic resource] by Rötig, Agnès Mollet, Julie Rio, Marlène Munnich, Arnold Producer: 20070914 In: Mitochondrion vol. 7 Suppl Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Molecular diagnostics of mitochondrial disorders. [electronic resource] by Rötig, Agnès Lebon, Sophie Zinovieva, Elena Mollet, Julie Sarzi, Emmanuelle Bonnefont, Jean-Paul Munnich, Arnold Producer: 20050217 In: Biochimica et biophysica acta vol. 1659 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders. [electronic resource] by Mollet, Julie Giurgea, Irina Schlemmer, Dimitri Dallner, Gustav Chretien, Dominique Delahodde, Agnès Bacq, Delphine de Lonlay, Pascale Munnich, Arnold Rötig, Agnès Producer: 20070504 In: The Journal of clinical investigation vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizures. [electronic resource] by Mollet, Julie Delahodde, Agnès Serre, Valérie Chretien, Dominique Schlemmer, Dimitri Lombes, Anne Boddaert, Nathalie Desguerre, Isabelle de Lonlay, Pascale de Baulny, Hélène Ogier Munnich, Arnold Rötig, Agnès Producer: 20080328 In: American journal of human genetics vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Germline gain-of-function mutations of ALK disrupt central nervous system development. [electronic resource] by de Pontual, Loïc Kettaneh, Dania Gordon, Christopher T Oufadem, Myriam Boddaert, Nathalie Lees, Melissa Balu, Laurent Lachassinne, Eric Petros, Andy Mollet, Julie Wilson, Louise C Munnich, Arnold Brugière, Laurence Delattre, Olivier Vekemans, Michel Etchevers, Heather Lyonnet, Stanislas Janoueix-Lerosey, Isabelle Amiel, Jeanne Producer: 20120327 In: Human mutation vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)