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	1.	Mutation detection in four candidate genes (OXA1L, MRS2L, YME1L and MIPEP) for combined deficiencies in the oxidative phosphorylation system. [electronic resource] by Coenen, M J H Smeitink, J A M Smeets, R Trijbels, F J M van den Heuvel, L P Producer: 20060705 In: Journal of inherited metabolic disease vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The first patient diagnosed with cytochrome c oxidase deficient Leigh syndrome: progress report. [electronic resource] by Coenen, M J H Smeitink, J A M Farhoud, M H Nijtmans, L G J Rodenburg, R Janssen, A van Kaauwen, E P M Trijbels, F J M van den Heuvel, L P Producer: 20061016 In: Journal of inherited metabolic disease vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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