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    Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I

    Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I by Barbara Cellini, Riccardo Montioli, Alessandro Paiardini, Antonio Lorenzetto, Fabio Maset, Tiziana Bellini, Elisa Oppici, Carla Borri Voltattorni

    Published 2010
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