(Q34668872)

English

Non-HFE haemochromatosis

scientific article

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scholarly article

1 reference

Europe PubMed Central

3 August 2017

1 reference

Europe PubMed Central

Non-HFE haemochromatosis (English)

1 reference

Europe PubMed Central

3 August 2017

author name string

Daniel-F Wallace

1

1 reference

Europe PubMed Central

3 August 2017

V-Nathan Subramaniam

2

1 reference

Europe PubMed Central

3 August 2017

language of work or name

0 references

publication date

1 September 2007

1 reference

Europe PubMed Central

3 August 2017

World Journal of Gastroenterology

1 reference

Europe PubMed Central

3 August 2017

13

1 reference

Europe PubMed Central

3 August 2017

35

1 reference

Europe PubMed Central

3 August 2017

4690-4698

1 reference

Europe PubMed Central

3 August 2017

Genetic background of primary iron overload syndromes in Japan

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Bone morphogenetic proteins 2, 4, and 9 stimulate murine hepcidin 1 expression independently of Hfe, transferrin receptor 2 (Tfr2), and IL-6

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Ferroportin (Q248H) mutations in African families with dietary iron overload

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

A mouse model of juvenile hemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Hemojuvelin is essential for dietary iron sensing, and its mutation leads to severe iron overload

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

First phenotypic description of transferrin receptor 2 knockout mouse, and the role of hepcidin.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Identification of ferroportin disease in the Indian subcontinent.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Recent advances in understanding haemochromatosis: a transition state

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Expression of hepcidin is down-regulated in TfR2 mutant mice manifesting a phenotype of hereditary hemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Analysis of genes implicated in iron regulation in individuals presenting with primary iron overload

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Spectrum of hemojuvelin gene mutations in 1q-linked juvenile hemochromatosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

HAMP as a modifier gene that increases the phenotypic expression of the HFE pC282Y homozygous genotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Genotypic and phenotypic heterogeneity of African Americans with primary iron overload

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Ferroportin 1 (SCL40A1) variant associated with iron overload in African-Americans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Iron overload in Africans and African-Americans and a common mutation in the SCL40A1 (ferroportin 1) gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Screening hepcidin for mutations in juvenile hemochromatosis: identification of a new mutation (C70R)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Transferrin receptor 2 (TfR2) and HFE mutational analysis in non-C282Y iron overload: identification of a novel TfR2 mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Natural history of juvenile haemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

New mutations inactivating transferrin receptor 2 in hemochromatosis type 3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Molecular cloning of transferrin receptor 2. A new member of the transferrin receptor-like family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Global prevalence of putative haemochromatosis mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Idiopathic hemochromatosis in a young female. A case study and review of the syndrome in young people

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

7 July 2018

Juvenile hemochromatosis caused by a novel combination of hemojuvelin G320V/R176C mutations in a 5-year old girl.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Targeted disruption of the hepatic transferrin receptor 2 gene in mice leads to iron overload.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Molecular mechanism of hepcidin deficiency in a patient with juvenile hemochromatosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Disparate phenotypic expression of ALAS2 R452H (nt 1407 G --> A) in two brothers, one with severe sideroblastic anemia and iron overload, hepatic cirrhosis, and hepatocellular carcinoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

A juvenile hemochromatosis patient homozygous for a novel deletion of cDNA nucleotide 81 of hemojuvelin.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Hemochromatosis and severe iron overload associated with compound heterozygosity for TFR2 R455Q and two novel mutations TFR2 R396X and G792R.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Genetic and clinical heterogeneity of ferroportin disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Effect of ferroportin Q248H polymorphism on iron status in African children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

A Portuguese patient homozygous for the -25G>A mutation of the HAMP promoter shows evidence of steady-state transcription but fails to up-regulate hepcidin levels by iron

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

A novel ferroportin mutation in a Canadian family with autosomal dominant hemochromatosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Primary iron overload with inappropriate hepcidin expression in V162del ferroportin disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Ferroportin disease due to the A77D mutation in Australia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Hemochromatosis with mutation of the ferroportin 1 (IREG1) gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Two novel mutations, L490R and V561X, of the transferrin receptor 2 gene in Japanese patients with hemochromatosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical features

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Homozygosity for a novel nonsense mutation (G66X) of the HJV gene causes severe juvenile hemochromatosis with fatal cardiomyopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Hepcidin is decreased in TFR2 hemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Hemojuvelin (HJV) mutations in persons of European, African-American and Asian ancestry with adult onset haemochromatosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Severe hemochromatosis in a Portuguese family associated with a new mutation in the 5'-UTR of the HAMP gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Early onset hereditary hemochromatosis resulting from a novel TFR2 gene nonsense mutation (R105X) in two siblings of north French descent.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Identification of a novel mutation (C321X) in HJV.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

A homozygous HAMP mutation in a multiply consanguineous family with pseudo-dominant juvenile hemochromatosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Type 3 hemochromatosis and beta-thalassemia trait

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Autosomal dominant iron overload due to a novel mutation of ferroportin1 associated with parenchymal iron loading and cirrhosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

HAMP gene mutation c.208T>C (p.C70R) identified in an Italian patient with severe hereditary hemochromatosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Homozygosity for transferrin receptor-2 Y250X mutation induces early iron overload.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Genetic abnormalities and juvenile hemochromatosis: mutations of the HJV gene encoding hemojuvelin.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Novel mutation in ferroportin 1 gene is associated with autosomal dominant iron overload

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Molecular analyses of patients with hyperferritinemia and normal serum iron values reveal both L ferritin IRE and 3 new ferroportin (slc11A3) mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Autosomal dominant reticuloendothelial iron overload (HFE type 4) due to a new missense mutation in the FERROPORTIN 1 gene (SLC11A3) in a large French-Canadian family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

26 October 2018

Hereditary hemochromatosis in adults without pathogenic mutations in the hemochromatosis gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4611190

9 December 2018

Genetic heterogeneity underlies juvenile hemochromatosis phenotype: analysis of three families of northern Greek origin

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant hereditary hemochromatosis associated with two novel Ferroportin 1 mutations in Spain

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The recently identified type 2A juvenile haemochromatosis gene (HJV), a second candidate modifier of the C282Y homozygous phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial iron overload with possible autosomal dominant inheritance

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of New Mutations of the HFE, Hepcidin, and Transferrin Receptor 2 Genes by Denaturing HPLC Analysis of Individuals with Biochemical Indications of Iron Overload

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of new mutations of hepcidin and hemojuvelin in patients with HFE C282Y allele

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous p.M172K mutation of the TFR2 gene in an Italian family with type 3 hereditary hemochromatosis and early onset iron overload

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Juvenile hemochromatosis associated with pathogenic mutations of adult hemochromatosis genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Iron overload and prolonged ingestion of iron supplements: clinical features and mutation analysis of hemochromatosis-associated genes in four cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Japanese family with ferroportin disease caused by a novel mutation of SLC40A1 gene: hyperferritinemia associated with a relatively low transferrin saturation of iron

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of enterocyte iron accumulation in the ferroportin disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Juvenile hemochromatosis HJV-related revealed by cardiogenic shock

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HJV gene mutations in European patients with juvenile hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

AVAQ 594-597 deletion of the TfR2 gene in a Japanese family with hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterogeneity of hemochromatosis in Italy

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and pathologic findings in hemochromatosis type 3 due to a novel mutation in transferrin receptor 2 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three patients with middle-age-onset hemochromatosis caused by novel mutations in the hemojuvelin gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Juvenile and adult hemochromatosis are distinct genetic disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hemojuvelin (HJV)-associated hemochromatosis: analysis of HJV and HFE mutations and iron overload in three families

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Juvenile hemochromatosis due to G320V/Q116X compound heterozygosity of hemojuvelin in an Irish patient

1 reference

https://pubmed.ncbi.nlm.nih.gov/17729390

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.3748/WJG.V13.I35.4690

1 reference

Europe PubMed Central

3 August 2017

1 reference

Europe PubMed Central

3 August 2017

1 reference

Europe PubMed Central

3 August 2017

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