D W Swinkels1, M P Cooreman, W W van Solinge
1Centraal Klinisch-chemisch Laboratorium, Academisch Ziekenhuis, Nijmegen.
Hereditary haemochromatosis (HHC) is a common iron absorption disorder. Identifying the Cys282Tyr mutation in the HFE gene aids early diagnosis and treatment of HHC.
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