Enzymological and mutational analysis of a complex primary hyperoxaluria type I phenotype involving alanine:Glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting and intraperoxisomal aggregation

C. J. Danpure, P. E. Purdue, P. Fryer, S. Griffiths, J. Allsop, M. J. Lumb, K. M. Guttridge, P. R. Jennings, J. I. Scheinman, S. M. Mauer, N. O. Davidson

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