A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient

Background: A severe form of iron overload with the clinicopathological features of haemochromatosis inherited in an autosomal dominant manner has been described in the Solomon Islands. The genetic basis of the disorder has not been identified. The disorder has similarities to type 4 haemochromatosi...

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Hlavní autoři: Arden, K E, Wallace, D F, Dixon, J L, Summerville, L, Searle, J W, Anderson, G J, Ramm, G A, Powell, L W, Subramaniam, V N
Médium: Artigo
Jazyk:Inglês
Vydáno: Copyright 2003 by Gut 2003
Témata:
Case Reports
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1773758/
https://ncbi.nlm.nih.gov/pubmed/12865285
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