Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2002-2-11
pubmed:abstractText
We analyzed the hepcidin gene in 10 Italian patients with hemochromatosis not related to C282Y, H63D or other less frequent HFE mutations, nor to Y250X in TFR2. The sequencing of the whole hepcidin coding region, intron-exon junctions, 5' and partially 3'UTRs, did not reveal any alteration in the studied patients.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0390-6078
pubmed:author
pubmed:issnType
Print
pubmed:volume
87
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
221-2
pubmed:dateRevised
2005-11-17
pubmed:meshHeading
pubmed-meshheading:11836175-Adult, pubmed-meshheading:11836175-Aged, pubmed-meshheading:11836175-Antimicrobial Cationic Peptides, pubmed-meshheading:11836175-DNA Mutational Analysis, pubmed-meshheading:11836175-DNA-Binding Proteins, pubmed-meshheading:11836175-Female, pubmed-meshheading:11836175-Genetic Predisposition to Disease, pubmed-meshheading:11836175-Genotype, pubmed-meshheading:11836175-HLA Antigens, pubmed-meshheading:11836175-Hemochromatosis, pubmed-meshheading:11836175-Histocompatibility Antigens Class I, pubmed-meshheading:11836175-Humans, pubmed-meshheading:11836175-Italy, pubmed-meshheading:11836175-Male, pubmed-meshheading:11836175-Membrane Proteins, pubmed-meshheading:11836175-Middle Aged, pubmed-meshheading:11836175-Point Mutation, pubmed-meshheading:11836175-Polymerase Chain Reaction, pubmed-meshheading:11836175-Transcription Factors, pubmed-meshheading:11836175-Upstream Stimulatory Factors
pubmed:year
2002
pubmed:articleTitle
Absence of hepcidin gene mutations in 10 Italian patients with primary iron overload.
pubmed:publicationType
Letter