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

BACKGROUND: Elevated serum ferritin levels are frequently encountered in clinical situations and once iron overload or inflammation has been ruled out, many cases remain unexplained. Genetic causes of hyperferritinemia associated to early cataract include mutations in the iron responsive element in...

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Bibliografische gegevens
Hoofdauteurs: Kannengiesser, Caroline, Jouanolle, Anne-Marie, Hetet, Gilles, Mosser, Annick, Muzeau, Françoise, Henry, Dominique, Bardou-Jacquet, Edouard, Mornet, Martine, Brissot, Pierre, Deugnier, Yves, Grandchamp, Bernard, Beaumont, Carole
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Ferrata Storti Foundation 2009
Onderwerpen:
Disorders of Iron Metabolism
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2649359/
https://ncbi.nlm.nih.gov/pubmed/19176363
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2008.000125
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