rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
3
|
pubmed:dateCreated |
2010-2-17
|
pubmed:abstractText |
Hypocaeruloplasminaemia can lead to tissue iron storage in Wilson's disease and the possibility of iron overload in long-term overtreated patients should be considered. The HFE gene encodes a protein that is intimately involved in intestinal iron absorption.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
1878-3562
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pubmed:author |
|
pubmed:copyrightInfo |
2009. Published by Elsevier Ltd.
|
pubmed:issnType |
Electronic
|
pubmed:volume |
42
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
216-9
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pubmed:meshHeading |
pubmed-meshheading:19640812-Adult,
pubmed-meshheading:19640812-Hepatolenticular Degeneration,
pubmed-meshheading:19640812-Histocompatibility Antigens Class I,
pubmed-meshheading:19640812-Humans,
pubmed-meshheading:19640812-Iron Overload,
pubmed-meshheading:19640812-Italy,
pubmed-meshheading:19640812-Male,
pubmed-meshheading:19640812-Membrane Proteins,
pubmed-meshheading:19640812-Mutation,
pubmed-meshheading:19640812-Prevalence,
pubmed-meshheading:19640812-Young Adult
|
pubmed:year |
2010
|
pubmed:articleTitle |
HFE gene mutations and Wilson's disease in Sardinia.
|
pubmed:affiliation |
Department of Gastroenterology, Azienda Ospedaliero - Universitaria of Cagliari, Italy. fiordo@tiscali.it
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pubmed:publicationType |
Journal Article
|