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pubmed-article:17710675pubmed:abstractTextHereditary aceruloplasminemia is an adult-onset autosomal recessive disease characterized by increased iron overload in the liver, pancreas, retina, and central nervous system. So far, 45 families with cases of aceruloplasminemia have been reported world-wide and mainly missense and nonsense mutations in the ceruloplasmin gene were detected.lld:pubmed
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pubmed-article:17710675pubmed:articleTitleIdentification and in silico characterization of a novel compound heterozygosity associated with hereditary aceruloplasminemia.lld:pubmed
pubmed-article:17710675pubmed:affiliationKlinik für Innere Medizin II, Kirrbergerstrasse, Universitätsklinikum des Saarlandes, Homburg, Germany.lld:pubmed
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