rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
12
|
pubmed:dateCreated |
1999-5-27
|
pubmed:abstractText |
The aim of our study was to evaluate the prevalence of Cys282Tyr mutation in patients with genetic haemochromatosis (GH) in Cantabria.
|
pubmed:language |
spa
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0025-7753
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
10
|
pubmed:volume |
112
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
451-3
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:10320958-Base Sequence,
pubmed-meshheading:10320958-Cysteine,
pubmed-meshheading:10320958-DNA Primers,
pubmed-meshheading:10320958-Female,
pubmed-meshheading:10320958-Gene Frequency,
pubmed-meshheading:10320958-Genotype,
pubmed-meshheading:10320958-Hemochromatosis,
pubmed-meshheading:10320958-Humans,
pubmed-meshheading:10320958-Male,
pubmed-meshheading:10320958-Molecular Sequence Data,
pubmed-meshheading:10320958-Mutation,
pubmed-meshheading:10320958-Phenotype,
pubmed-meshheading:10320958-Polymerase Chain Reaction,
pubmed-meshheading:10320958-Prevalence,
pubmed-meshheading:10320958-Spain,
pubmed-meshheading:10320958-Tyrosine
|
pubmed:year |
1999
|
pubmed:articleTitle |
[The prevalence of the Cys282Tyr mutation in the hemochromatosis gene in Cantabria in patients diagnosed with hereditary hemochromatosis].
|
pubmed:affiliation |
Servicio de Aparato Digestivo, Hospital Universitario Marqués de Valdecilla, Santander.
|
pubmed:publicationType |
Journal Article,
English Abstract,
Research Support, Non-U.S. Gov't
|