Ferroportin mutation in autosomal dominant hemochromatosis: loss of function, gain in understanding

Ítems similars

• Hepcidin: A putative iron-regulatory hormone relevant to hereditary hemochromatosis and the anemia of chronic disease
  per: Fleming, Robert E., et al.
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• Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia
  per: Rock, Matthew J, et al.
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• Immunological loss-of-function due to genetic gain-of-function in humans: autosomal dominance of the third kind
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• Autosomal-dominant hemochrom-atosis is associated with a mutation in the ferroportin (SLC11A3) gene
  per: Montosi, Giuliana, et al.
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• Loss-of-function Mutation in PMVK Causes Autosomal Dominant Disseminated Superficial Porokeratosis
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