Associated Papers
Genetic heterogeneity in primary hyperoxaluria type 1: impact on diagnosis.
Coulter-Mackie MB et al.
Molecular Genetics and Metabolism, 0
Molecular etiology of primary hyperoxaluria type 1: new directions for treatment.
Danpure CJ
American Journal of Nephrology, 0
The major allele of the alanine:glyoxylate aminotransferase gene: nine novel mutations and polymorphisms associated with primary hyperoxaluria type 1.
Coulter-Mackie MB et al.
Molecular Genetics and Metabolism, 0
Select a paper to view details