Associated Papers
Molecular insights into primary hyperoxaluria type 1 pathogenesis.
Cellini B et al.
Frontiers in Bioscience (landmark Edition), 2012
Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I.
Cellini B et al.
Proceedings of the National Academy of Sciences of the United States of America, 2010
Consequences of missense mutations for dimerization and turnover of alanine:glyoxylate aminotransferase: study of a spectrum of mutations.
Coulter-Mackie MB et al.
Molecular Genetics and Metabolism, 2006
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