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Structural Basis of Hereditary Coproporphyria von Lee, Dong-Sun, Flachsová, Eva, Bodnárová, Michaela, Demeler, Borries, Martásek, Pavel, Raman, C. S., Murad, Ferid

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De Novo mutation found in the porphobilinogen deaminase gene in Slovak acute intermittent porphyria patient: molecular biochemical study von Ulbrichova, D, Flachsova, E, Hrdinka, M, Saligova, J, Bazar, J, Raman, C S, Martasek, P

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De Novo mutation found in the porphobilinogen deaminase gene in slovak acute intermittent porphyria patient: molecular biochemical Study von Ulbrichova, D, Flachsova, E, Hrdinka, M, Saligova, J, Bazar, J, Raman, C S, Martasek, P

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De novo mutation found in the porphobilinogen deaminase gene in Slovak acute intermittent porphyria patient: Molecular biochemical study von Ulbrichova, D, Flachsova, E, Hrdinka, M, Saligova, J, Bazar, J, Raman, C.S, Martasek, P

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