Publication | Closed Access
Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine : glyoxylate aminotransferase gene
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Citations
3
References
1999
Year
Glyoxylate Aminotransferase GeneMendelian DisorderBiochemistryGenetic DisorderMedicineGeneticsInherited Metabolic DiseaseMolecular AnalysisHyperoxaluria Type 1Chronic Kidney Disease
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