Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Type 3 hereditary hemochromatosis in a patient from sub-Saharan Africa: is there a link between African iron overload and TFR2 dysfunction?

Blood cells, molecules & diseases - 1 Jan 2013

Majore Silvia, Ricerca Bianca Maria, Radio Francesca Clementina, Binni Francesco, Cosentino Ilaria, Gallusi Giulia, De Bernardo Carmelilia, Morrone Aldo, Grammatico Paola

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Africa South of the Sahara
Share to Amino Acid Sequence
Share to Anemia, Sideroblastic

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to Hemochromatosis

Share to Heterozygote

Share to Receptors, Transferrin

Share to Sequence Alignment

Source

Identifiers

PMID: 22981443
DOI: 10.1016/j.bcmd.2012.08.007

Genes

TFR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Type 3 hereditary hemochromatosis in a patient from sub-Saharan Africa: is there a link between African iron overload and TFR2 dysfunction?PMID 22981443Read ↗

TFR2-related haemochromatosis in the Netherlands: a cause of arthralgia in young adulthood.Semantic proximity Read ↗

Haemochromatosis.Semantic proximity Read ↗

Hereditary hemochromatosis: a review of the genetics, mechanism, diagnosis, and treatment of iron overload.Semantic proximity Read ↗

Early-onset haemochromatosis caused by a novel combination of TFR2 mutations(p.R396X/c.1538-2 A>G) in a woman of Italian descent.Semantic proximity Read ↗

Hemochromatosis: when blood is too iron-rich.Semantic proximity Read ↗

What is HFE haemochromatosis?Semantic proximity Read ↗

Genetic haemochromatosis: genes and mutations associated with iron loading.Semantic proximity Read ↗

HFE hemochromatosis in African Americans: Prevalence estimates of iron overload and iron overload-related disease.Semantic proximity Read ↗

Do hemochromatosis mutations protect against iron-mediated atherogenesis?Semantic proximity Read ↗

Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical featuresSemantic proximity Read ↗

HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overloadSemantic proximity Read ↗

Hereditary hemochromatosis and its elusive natural history.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.