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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
21
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pubmed:dateCreated |
2000-11-8
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pubmed:abstractText |
Hemochromatosis occurs in approximately 5 white people per 1000 and is usually due to homozygosity for mutations in the HLA-linked HFE gene. Although screening has been proposed, the proportion of homozygotes with conditions related to hemochromatosis is uncertain.
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pubmed:grant |
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0028-4793
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
23
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pubmed:volume |
343
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1529-35
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:11087882-Adult,
pubmed-meshheading:11087882-Family,
pubmed-meshheading:11087882-Female,
pubmed-meshheading:11087882-Hemochromatosis,
pubmed-meshheading:11087882-Homozygote,
pubmed-meshheading:11087882-Humans,
pubmed-meshheading:11087882-Iron Overload,
pubmed-meshheading:11087882-Liver Cirrhosis,
pubmed-meshheading:11087882-Male,
pubmed-meshheading:11087882-Middle Aged,
pubmed-meshheading:11087882-Prevalence,
pubmed-meshheading:11087882-Transaminases,
pubmed-meshheading:11087882-Transferrin
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pubmed:year |
2000
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pubmed:articleTitle |
Disease-related conditions in relatives of patients with hemochromatosis.
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pubmed:affiliation |
Department of Medicine, University of Utah School of Medicine, Salt Lake City, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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