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	1.	Hereditary haemochromatosis caused by homozygous HJV mutation evolved through paternal disomy. [electronic resource] by Neřoldová, M Fraňková, S Stránecký, V Honsová, E Lukšan, O Beneš, M Michalová, K Kmoch, S Jirsa, M Producer: 20150820 In: Clinical genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Large copy-number variations in patients with statin-associated myopathy affecting statin myopathy-related loci. [electronic resource] by Stránecký, V Neřoldová, M Hodaňová, K Hartmannová, H Piherová, L Zemánková, P Přistoupilová, A Vrablík, M Adámková, V Kmoch, S Jirsa, M Producer: 20170329 In: Physiological research vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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