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	1.	Identical germ-line mutations in the triosephosphate isomerase alleles of two brothers are associated with distinct clinical phenotypes. [electronic resource] by Valentin, C Cohen-Solal, M Maquat, L Horányi, M Inselt-Kovács, M Hollán, S Producer: 20000519 In: Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie vol. 323 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	[Glycolytic enzyme defects and neurodegeneration]. [electronic resource] by Hollán, S Vécsei, L Karg, E Németh, I Horanyi, M Inselt-Kovács, M Farkas, T Producer: 19990128 In: Comptes rendus des seances de la Societe de biologie et de ses filiales vol. 192 Availability: No items available. Save to lists Add to cart (remove)
	3.	Hereditary triosephosphate isomerase (TPI) deficiency: two severely affected brothers one with and one without neurological symptoms. [electronic resource] by Hollán, S Fujii, H Hirono, A Hirono, K Karro, H Miwa, S Harsányi, V Gyódi, E Inselt-Kovács, M Producer: 19940105 In: Human genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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