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	1.	Novel pathogenic SLC25A46 splice-site mutation causes an optic atrophy spectrum disorder. [electronic resource] by Nguyen, M Boesten, I Hellebrekers, D M E I Mulder-den Hartog, N M de Coo, I F M Smeets, H J M Gerards, M Producer: 20170613 In: Clinical genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	PGD and heteroplasmic mitochondrial DNA point mutations: a systematic review estimating the chance of healthy offspring. [electronic resource] by Hellebrekers, D M E I Wolfe, R Hendrickx, A T M de Coo, I F M de Die, C E Geraedts, J P M Chinnery, P F Smeets, H J M Producer: 20130923 In: Human reproduction update vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Defective NDUFA9 as a novel cause of neonatally fatal complex I disease. [electronic resource] by van den Bosch, B J C Gerards, M Sluiter, W Stegmann, A P A Jongen, E L C Hellebrekers, D M E I Oegema, R Lambrichs, E H Prokisch, H Danhauser, K Schoonderwoerd, K de Coo, I F M Smeets, H J M Producer: 20120410 In: Journal of medical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	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)