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	1.	A novel NDUFV1 gene mutation in complex I deficiency in consanguineous siblings with brainstem lesions and Leigh syndrome. [electronic resource] by Vilain, C Rens, C Aeby, A Balériaux, D Van Bogaert, P Remiche, G Smet, J Van Coster, R Abramowicz, M Pirson, I Producer: 20130705 In: Clinical genetics vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Genetic polymorphisms in UDP-glucuronosyltransferase 1A6 and 1A7 and the risk for benign Warthin's tumors of the parotid gland. [electronic resource] by Lacko, Martin Voogd, Adri C van de Goor, Rens C E Roelofs, Hennie M J Te Morsche, Rene H M Bouvy, Nicole D Peters, Wilbert H M Manni, Johannes J Producer: 20180227 In: Head & neck vol. 38 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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