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	1.	Molecular Diagnostics of Copper-Transporting Protein Mutations Allows Early Onset Individual Therapy of Menkes Disease. [electronic resource] by Králík, L Flachsová, E Hansíková, H Saudek, V Zeman, J Martásek, P Producer: 20180917 In: Folia biologica vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	De Novo mutation found in the porphobilinogen deaminase gene in Slovak acute intermittent porphyria patient: molecular biochemical study. [electronic resource] by Ulbrichova, D Flachsova, E Hrdinka, M Saligova, J Bazar, J Raman, C S Martasek, P Producer: 20070529 In: Physiological research vol. 55 Suppl 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A new mutation within the porphobilinogen deaminase gene leading to a truncated protein as a cause of acute intermittent porphyria in an extended Indian family. [electronic resource] by Flachsová, E Verma, I C Ulbrichová, D Saxena, R Zeman, J Saudek, V Raman, C S Martásek, P Producer: 20080116 In: Folia biologica vol. 53 Availability: No items available. Save to lists Add to cart (remove)

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