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Results: 1-2 |
Results: 2
A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renalglycogenosis with Fanconi syndrome and low phosphorylase kinase activity
Authors: Burwinkel, B Sanjad, SA Al-Sabban, E Al-Abbad, A Kilimann, MW
Citation: B. Burwinkel et al., A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renalglycogenosis with Fanconi syndrome and low phosphorylase kinase activity, HUM GENET, 105(3), 1999, pp. 240-243
Primary hyperoxaluria type I: An underestimated cause of nephrocalcinosis and chronic renal failure in Saudi Arabian children
Authors: Sanjad, SA Al-Abbad, A Al-Sabban, E
Citation: Sa. Sanjad et al., Primary hyperoxaluria type I: An underestimated cause of nephrocalcinosis and chronic renal failure in Saudi Arabian children, ANN SAUDI M, 19(1), 1999, pp. 4-7
Risultati: 1-2 |