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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
2006-7-31
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pubmed:abstractText |
Hemochromatosis is a common inherited disorder of iron metabolism and one of the most important causes of iron overload. The objective was to analyze the presence of C282Y, H63D and S65C mutations in the HFE gene and HLA-A alleles for a group of Brazilian patients with iron overload, and to correlate genotype with clinical and laboratory variables.
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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 |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1516-3180
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
2
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pubmed:volume |
124
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
55-60
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pubmed:dateRevised |
2008-2-28
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pubmed:meshHeading |
pubmed-meshheading:16878186-Adult,
pubmed-meshheading:16878186-Aged,
pubmed-meshheading:16878186-Alleles,
pubmed-meshheading:16878186-Female,
pubmed-meshheading:16878186-Genetic Markers,
pubmed-meshheading:16878186-Genotype,
pubmed-meshheading:16878186-HLA-A Antigens,
pubmed-meshheading:16878186-Hemochromatosis,
pubmed-meshheading:16878186-Histocompatibility Antigens Class I,
pubmed-meshheading:16878186-Humans,
pubmed-meshheading:16878186-Iron Overload,
pubmed-meshheading:16878186-Male,
pubmed-meshheading:16878186-Membrane Proteins,
pubmed-meshheading:16878186-Middle Aged,
pubmed-meshheading:16878186-Mutation,
pubmed-meshheading:16878186-Polymerase Chain Reaction,
pubmed-meshheading:16878186-Prospective Studies
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pubmed:year |
2006
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pubmed:articleTitle |
Analysis of HFE gene mutations and HLA-A alleles in Brazilian patients with iron overload.
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pubmed:affiliation |
Department of Internal Medicine, Faculdade de Ciências Médicas da Santa Casa de Misericórdia de São Paulo, São Paulo, Brazil. rdcan@uol.com.br
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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