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14, 223238 (Springer, 1996)
The disease is caused by a mutation in the ATP7B gene, which codes for a protein that facilitates the incorporation of copper into proteins (such as ceruloplasmin) and also the transportation of copper into vesicles that allow it to be secreted in bile.1 The critical effect of a mutation in ATP7B is diminished copper secretion into bile, which leads to excess copper accumulation in the hepatocyte
Circulation 133 (19), 18511860
Los deportistas, aficionados o profesionales, as como los que siguen un rgimen de adelgazamiento, pueden beneficiarse de un aporte suplementario de L-carnitina
Vitamin C : A potent antioxidant, vitamin C aids in collagen production, improves skin elasticity, and helps in fading hyperpigmentation