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	1.	NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect. [electronic resource] by Baertling, F Sánchez-Caballero, L van den Brand, M A M Fung, C-W Chan, S H-S Wong, V C-N Hellebrekers, D M E de Coo, I F M Smeitink, J A M Rodenburg, R J T Nijtmans, L G J Producer: 20180806 In: Clinical genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy. [electronic resource] by Jonckheere, A I Hogeveen, M Nijtmans, L G J van den Brand, M A M Janssen, A J M Diepstra, J H S van den Brandt, F C A van den Heuvel, L P Hol, F A Hofste, T G J Kapusta, L Dillmann, U Shamdeen, M G Smeitink, J A M Rodenburg, R J T Producer: 20080403 In: Journal of medical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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