A new missense mutation in the L ferritin coding sequence associated with elevated levels of glycosylated ferritin in serum and absence of iron overload

Lignende værker

• A New Pathogenic Missense Variant in a Consanguineous North-African Family Responsible for a Highly Variable Aceruloplasminemia Phenotype: A Case-Report
  af: Hervé Lobbes, et al.
  Udgivet: (2022-05-01)
• Both Hepatic and Body Iron Stores Are Increased in Dysmetabolic Iron Overload Syndrome. A Case-Control Study
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  Udgivet: (2015)
• Determination of Serum Ferritin Glycosylation in Hyperferritinemia Associated to Iron Overload and Inflammation.
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  Udgivet: (2009)
• A new mutation in the hepcidin promoter impairs its BMP response and contributes to a severe phenotype in HFE related hemochromatosis
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• HAMP promoter mutation nc.-153 C>T in 785 HEIRS Study participants: author reply
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  Udgivet: (2009)