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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 |
2003-2-25
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pubmed:abstractText |
Hereditary hemochromatosis (HH) is characterized by excess iron deposition. Two mutations in the HFE gene are associated with HH. Heterozygous carriers of HFE mutations are at higher risk of developing type 2 diabetes mellitus (T2DM). The aims of our project were to identify the frequency of C282Y and H63D mutations in a population from the Ma?opolska region of south-eastern Poland, and to search for an association of HFE mutations with T2DM.
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pubmed:grant |
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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 |
Feb
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pubmed:issn |
1234-1010
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
9
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
BR91-5
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:12601293-Adult,
pubmed-meshheading:12601293-Aged,
pubmed-meshheading:12601293-Case-Control Studies,
pubmed-meshheading:12601293-Diabetes Mellitus, Type 2,
pubmed-meshheading:12601293-Female,
pubmed-meshheading:12601293-Gene Frequency,
pubmed-meshheading:12601293-Genotype,
pubmed-meshheading:12601293-Hemochromatosis,
pubmed-meshheading:12601293-Histocompatibility Antigens Class I,
pubmed-meshheading:12601293-Humans,
pubmed-meshheading:12601293-Male,
pubmed-meshheading:12601293-Membrane Proteins,
pubmed-meshheading:12601293-Middle Aged,
pubmed-meshheading:12601293-Point Mutation,
pubmed-meshheading:12601293-Poland
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pubmed:year |
2003
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pubmed:articleTitle |
A search for association between hereditary hemochromatosis HFE gene mutations and type 2 diabetes mellitus in a Polish population.
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pubmed:affiliation |
Department of Metabolic Diseases, Medical College, Jagellonian University, Cracow, Poland. mmalecki@cm-uj.krakow.pl
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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