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doi: 10.1111/j.1748-1716.1993.tb09513.x
Rethinking cystic fibrosis pathology: The critical role of abnormal reduced glutathione (GSH) transport caused by CFTR mutation
Both hyperuricemia and renal disposition of uric acid are polygenic traits and multiple haplotypes of renal urate transporters are increasingly recognized as significant factors
Thiamine (Vitamin B1) aids in carbohydrate metabolism and energy production
