Hereditary hemochromatosis in liver transplantation
M. Isabel Fiel, Thomas D. Schiano, Henry C. Bodenheimer, Swan N. Thung, Thomas W. King, C. Rathna Varma, Charles M. Miller, Elizabeth M. Brunt, Steven Starnes, Cynthia Prass, Roger K. Wolff, Bruce R. Bacon – 30 December 2003 – A candidate gene, HFE, was recently described in patients with hereditary hemochromatosis (HH) and found to contain a missense mutation leading to a cysteine to tyrosine substitution (C282Y). A second mutation, H63D, was also found in the gene.