Two cohorts of referred hemochromatosis probands with HFE p.C282Y/p.C282Ya.

Figshare2024-05-14 更新2026-04-28 收录

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https://figshare.com/articles/dataset/Two_cohorts_of_referred_hemochromatosis_probands_with_i_HFE_i_p_C282Y_p_C282Y_sup_a_sup_/25819610 数据链接链接失效反馈

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Two cohorts of referred hemochromatosis probands with HFE p.C282Y/p.C282Ya.

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2024-05-14

Dataset: Serum IgA and IgM levels in referred hemochromatosis probands with HFE p.C282Y/p.C282Y

遗传性血色素沉着症

免疫球蛋白

Aims of this retrospective study were: 1) to compile serum IgA and IgM levels at diagnosis in a cohort of 73 Alabama referred hemochromatosis probands with HFE p.C282Y homozygosity and HLA-A ty

DataCite Commons2024-08-16 更新80

Average values of total body iron stores (TBIS) and serum ferritin (SF) of HH male patients according to the associated SNP microhaplotypes (A-A-T homozygous or non- A-A-T homozygous).

遗传性血色素沉着症

铁代谢基因型关联

TBIS and SF are presented as geometric mean and 95% Confidence Interval for Mean [Lower Bound - Upper Bound]; the numbers of patients in each group (n) are indicated in each case. *(P) Statistical sig

NIAID Data Ecosystem60

Incidence of a clinically relevant H63D syndrome in carriers of a homozygous mutation of HFE gene H63D

HFE基因突变

铁过载疾病

H63D syndrome is a phenotype of a homozygous mutation of the HFE gene H63D, which is otherwise known to cause at most mild classical hemochromatosis. H63D syndrome leads to an iron overload in the bod

DataCite Commons2024-10-24 更新20

Iron uptake from plasma transferrin by the duodenum is impaired in the Hfe knockout mouse

铁代谢机制

遗传性血色素沉着症

Hereditary hemochromatosis (HH) is a disorder of iron metabolism in which enhanced iron absorption of dietary iron causes increased iron accumulation in the liver, heart, and pancreas. Most individual

PubMed Central2002-04-09 更新60

Table S1 - Effects of Highly Conserved Major Histocompatibility Complex (MHC) Extended Haplotypes on Iron and Low CD8 + T Lymphocyte Phenotypes in HFE C282Y Homozygous Hemochromatosis Patients from Three Geographically Distant Areas

遗传性血色素沉着症

HLA基因

Comparison of the most common HLA allele, HLA A–B haplotype (uncorrected data) and SNP microhaplotype frequencies among three different populations of HH patients. (DOCX)

NIAID Data Ecosystem50

Two cohorts of referred hemochromatosis probands with HFE p.C282Y/p.C282Ya.

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