The significance of the 187G (H63D) mutation in hemochromatosis.
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Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) geneAllele frequencies of hemojuvelin gene (HJV) I222N and G320V missense mutations in white and African American subjects from the general Alabama populationAssociation between hemochromatosis genotype and lead exposure among elderly men: the normative aging studyHFE H63D mutation frequency shows an increase in Turkish women with breast cancerHemochromatosis gene in leukemia and lymphomaThe global prevalence of HFE and non-HFE hemochromatosis estimated from analysis of next-generation sequencing data.Iron overload is rare in patients homozygous for the H63D mutationThe effect of the hemochromatosis (HFE) genotype on lead load and iron metabolism among lead smelter workers.Non-viral causes of hepatocellular carcinoma.Frequency of primary iron overload and HFE gene mutations (C282Y, H63D and S65C) in chronic liver disease patients in north India.Molecular diagnosis of hemochromatosis.Contribution of the H63D mutation in HFE to murine hereditary hemochromatosis.Variable phenotypic presentation of iron overload in H63D homozygotes: are genetic modifiers the cause?Targeted disruption of the HFE geneHFE gene mutations in susceptibility to childhood leukemia: HuGE review.Heritability of serum iron measures in the hemochromatosis and iron overload screening (HEIRS) family studyHereditary haemochromatosis as an immunological disease.Homogeneous multiplex genotyping of hemochromatosis mutations with fluorescent hybridization probes.Molecular biology and the diagnosis and treatment of liver diseases.Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.HFE based re-evaluation of heterozygous hemochromatosis.Lack of association of primary iron overload and common HFE gene mutations with liver cirrhosis in adult Indian population.Significance of H63D homozygosity in a Basque population with hemochromatosis.
P2860
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P2860
The significance of the 187G (H63D) mutation in hemochromatosis.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh-hant
name
The significance of the 187G (H63D) mutation in hemochromatosis.
@en
The significance of the 187G
@nl
type
label
The significance of the 187G (H63D) mutation in hemochromatosis.
@en
The significance of the 187G
@nl
prefLabel
The significance of the 187G (H63D) mutation in hemochromatosis.
@en
The significance of the 187G
@nl
P2860
P1476
The significance of the 187G (H63D) mutation in hemochromatosis.
@en
P2093
P2860
P304
P356
10.1016/S0002-9297(07)64339-0
P407
P577
1997-09-01T00:00:00Z