AUB ScholarWorks

Browsing Faculty of Medicine (FM) by Subject "C282Y"

Browsing Faculty of Medicine (FM) by Subject "C282Y"

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  • Mahfouz R.A.R.; Sarieddine D.S.; Charafeddine K.M.; Abdul Khalik R.N.; Cortas N.K.; Daher R.T. (DORDRECHTVAN GODEWIJCKSTRAAT 30, 3311 GZ DORDRECHT, NETHERLANDS, 2012)
    Hereditary hemochromatosis (HHC) is a genetic disorder of iron metabolism characterized by abnormal accumulation of iron that may lead to organ damage and death. Diagnosis is usually based on various genetic and phenotypic ...
  • Daher R.T.; Khalik R.N.A.; Hoteit R.M.; Sarieddine D.S.; Charafeddine K.M.; Cortas N.K.; Mahfouz R.A.R. (NEW ROCHELLE140 HUGUENOT STREET, 3RD FL, NEW ROCHELLE, NY 10801 USA, 2011)
    Aims: Hereditary hemochromatosis (HHC) is the most commonly identified autosomal recessive genetic disorder in the Caucasian population and HFE gene mutations are highly concentrated among European populations. This is the ...

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