about
Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosisRecent advances in understanding haemochromatosis: a transition stateAllele frequencies of hemojuvelin gene (HJV) I222N and G320V missense mutations in white and African American subjects from the general Alabama populationMusculoskeletal complications of haematological diseaseThe gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22.Sequence variation and haplotype structure at the human HFE locus.Haemochromatosis: iron still matters.Human leukocyte antigen haplotypes and HFE mutations in Spanish hereditary hemochromatosis and sporadic porphyria cutanea tarda.Haemochromatosis: understanding the mechanism of disease and implications for diagnosis and patient management following the recent cloning of novel genes involved in iron metabolism.Natural history of juvenile haemochromatosis.Molecular pathogenesis of iron overload.Hereditary hemochromatosis: perspectives of public health, medical genetics, and primary care.Genes that modify the hemochromatosis phenotype in mice.Current and future therapy in haemochromatosis and Wilson's disease.A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient.Hereditary hemochromatosis and transferrin receptor 2Hepcidin: what every gastroenterologist should know.Hereditary haemochromatosis.The molecular genetics of haemochromatosis.Hereditary iron and copper deposition: diagnostics, pathogenesis and therapeutics.Down-regulation of hepcidin in porphyria cutanea tardaA late presentation of a fatal disease: juvenile hemochromatosis.The Regulation of Iron Absorption and Homeostasis.Disorders associated with systemic or local iron overload: from pathophysiology to clinical practice.Iron storage disease in Asia-Pacific populations: the importance of non-HFE mutations.Interaction of hemojuvelin with neogenin results in iron accumulation in human embryonic kidney 293 cells.Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis.High prevalence of non-HFE gene-associated haemochromatosis in patients from southern Italy.A juvenile hemochromatosis patient homozygous for a novel deletion of cDNA nucleotide 81 of hemojuvelin.Of mice and men: genetic determinants of iron status.The mechanisms of systemic iron homeostasis and etiology, diagnosis, and treatment of hereditary hemochromatosis.Analysis of haemochromatosis gene mutations in a population from the Mediterranean Basin.Hepatic failure and hemochromatosis of Salers and Salers-cross cattle.Heritability of Serum Iron, Ferritin and Transferrin Saturation in a Genetically Isolated Population, the Erasmus Rucphen Family (ERF) StudyJuvenile hemochromatosis locus maps to chromosome 1q in a French Canadian populationInherited Disorders of Iron Overload
P2860
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P2860
description
1999 nî lūn-bûn
@nan
1999 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Juvenile hemochromatosis locus maps to chromosome 1q
@nl
Juvenile hemochromatosis locus maps to chromosome 1q.
@ast
Juvenile hemochromatosis locus maps to chromosome 1q.
@en
type
label
Juvenile hemochromatosis locus maps to chromosome 1q
@nl
Juvenile hemochromatosis locus maps to chromosome 1q.
@ast
Juvenile hemochromatosis locus maps to chromosome 1q.
@en
prefLabel
Juvenile hemochromatosis locus maps to chromosome 1q
@nl
Juvenile hemochromatosis locus maps to chromosome 1q.
@ast
Juvenile hemochromatosis locus maps to chromosome 1q.
@en
P2093
P2860
P356
P1476
Juvenile hemochromatosis locus maps to chromosome 1q
@en
P2093
C Camaschella
G D'Ascola
M Cicilano
P Gasparini
P2860
P304
P356
10.1086/302379
P407
P577
1999-05-01T00:00:00Z