Associated Papers
AGXT gene mutations and their influence on clinical heterogeneity of type 1 primary hyperoxaluria.
Amoroso A et al.
Journal of the American Society of Nephrology : Jasn, 2001
Primary hyperoxaluria type 1: diagnostic relevance of mutations and polymorphisms in the alanine:glyoxylate aminotransferase gene (AGXT).
Tarn AC et al.
Journal of Inherited Metabolic Disease, 1997
Primary hyperoxaluria: genotype-phenotype correlation.
Pirulli D et al.
Journal of Nephrology, 0
Experience in prenatal diagnosis of primary hyperoxaluria type 1.
Rumsby G
Journal of Nephrology, 0
Molecular analysis of the AGXT gene in Italian patients with primary hyperoxaluria type 1 (PH1).
Ferrettini C et al.
Journal of Nephrology, 0
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