About: Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis

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About: Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis Goto Sponge NotDistinct Permalink

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scientific article published on 01 November 1997

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в листопаді 1997 (uk) article scientifique publié en 1997 (fr) im November 1997 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 01 November 1997 (en) artículu científicu espublizáu en payares de 1997 (ast)
publication date	wds:Q73908698-E2B69FD0-97B7-468B-9D17-DF8A2A51959E
publication date	1997-11-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q73908698-02E17F60-D177-40A8-BE49-18197CB7BB08 wds:Q73908698-24A0EB95-22E3-4FF0-ADF8-E860D1843D58 wds:Q73908698-37DF8630-37E0-4450-AFC3-0147C62DE36A wds:Q73908698-43B15473-1018-465D-B389-200BC4E6AE17 wds:Q73908698-4EF8FC02-34FB-454E-886C-9644B2B8C130 wds:Q73908698-6E311F12-7863-4D84-B094-1A6D7A7CD87E wds:Q73908698-84B69F96-41E6-48D3-AF4E-2571ABFCE584 wds:Q73908698-95786C45-6E13-4E60-AB77-010AF56899C9 wds:Q73908698-9D37CA44-FA26-4F2E-88FF-52520E60F361 wds:Q73908698-D5B319D1-7F35-4B5F-8953-51EA21BACFA3
cites work	Haemochromatosis and HLA-H. Haemochromatosis and HLA-H Mutation analysis in hereditary hemochromatosis. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis Survival and causes of death in cirrhotic and in noncirrhotic patients with primary hemochromatosis Association of HLA-A3 and HLA-B14 antigens with idiopathic haemochromatosis Long-term survival in patients with hereditary hemochromatosis New polymorphic microsatellite markers place the haemochromatosis gene telomeric to D6S105 Alleles at D6S265 and D6S105 define a haemochromatosis-specific genotype Idiopathic hemochromatosis, an interim report.
author name string	wds:Q73908698-1C652978-E27F-4303-9339-08F6752E8F43 wds:Q73908698-30BF43C8-93B5-44FF-9898-00BAEC7F6032 wds:Q73908698-38B45197-B04E-4D8C-8D45-D49CD35929C5 wds:Q73908698-3ACB77B1-34F8-4E8F-B51B-74A95AC619AC wds:Q73908698-3C05EA7B-B79E-4DC7-8151-A230DBFB07A3 wds:Q73908698-461B2D57-C78D-4EF6-9399-6E0A06A359CF wds:Q73908698-6B42703A-3DBF-4D1D-9177-94A3624A86CD wds:Q73908698-718D407E-3CC4-47F8-BB89-A4093468FBEE wds:Q73908698-8931F500-6B5A-4AC3-87ED-F93F19A071E5 wds:Q73908698-B1D494FF-6FBF-4FCE-8321-99A61103336D wds:Q73908698-BAB9B205-DBDF-4984-861B-2F7068F9BF59 wds:Q73908698-D606DA8E-429C-4251-96D5-716385E6941E wds:Q73908698-E6CA5191-5E30-4B35-9BCB-525586FD6838
author name string	C Datz P Ferenci W Vogel B Paulweber F Sandhofer I Graziadei F Hackl M R Lalloz A Bomford E Penner T Maier-Dobersberger D M Layton G Vautier
rdfs:label	Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis (en) Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis (nl)
skos:prefLabel	Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis (en) Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis (nl)
name	Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis (en) Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis (nl)
title	wds:Q73908698-0D0BD934-0827-4967-9546-2A3B646C068F
title	Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis (en)
page(s)	wds:Q73908698-758108F4-CB8E-4110-B316-3FED39EB0DCD
page(s)	773-779
instance of	wds:Q73908698-35C8F1CA-24B9-49F6-A233-C38D8C7BCE3D
instance of	scholarly article
PubMed ID	wds:Q73908698-30F473D7-4C03-4E15-98E5-76A47A100734
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9382962
PubMed ID	9382962
published in	wds:Q73908698-C619F471-2992-47FD-8F17-9B9AB205F1B8
published in	Journal of Hepatology
issue	wds:Q73908698-E40AFAEA-08AD-43AD-B78D-686FAC99E387
volume	wds:Q73908698-B6469A41-A502-4020-8896-EAAC4C4BF8C9
issue	5
volume	27
DOI	wds:Q73908698-B93E2319-8F11-4115-B88D-07A10FE61A6D
DOI	http://dx.doi.org/10.1016/S0168-8278(97)80312-1
DOI	10.1016/S0168-8278(97)80312-1
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73908698
is cites work of	Association of HFE protein with transferrin receptor in crypt enterocytes of human duodenum Evidence that the Cys282Tyr mutation of the HFE gene originated from a population in Southern Scandinavia and spread with the Vikings HFE gene mutation (C282Y) and phenotypic expression among a hospitalised population in a high prevalence area of haemochromatosis Mutations of the HFE gene in patients with hepatocellular carcinoma High prevalence of the hemochromatosis-associated Cys282Tyr HFE gene mutation in a healthy Norwegian population in the city of Oslo, and its phenotypic expression. Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls Frequency of the HFE C282Y and H63D mutations in Danish patients with clinical haemochromatosis initially diagnosed by phenotypic methods Genetics of haemochromatosis The relation of iron status and hemochromatosis gene mutations in patients with chronic hepatitis C Phenotypic expression of HFE mutations: a French study of 1110 unrelated iron-overloaded patients and relatives The evolutionary adaptation of the C282Y mutation to culture and climate during the European Neolithic A genotypic study of 217 unrelated probands diagnosed as "genetic hemochromatosis" on "classical" phenotypic criteria HFE-related hemochromatosis: an update for the rheumatologist HFE hemochromatosis screening in patients with severe hip osteoarthritis: A prospective cross-sectional study Frequency and biochemical expression of C282Y/H63D hemochromatosis (HFE) gene mutations in the healthy adult population in Italy Cloning, sequencing and characterization of the rat hereditary hemochromatosis promoter: comparison of the human, mouse and rat HFE promoter regions. EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH). [Osteoarthritis in hereditary metabolic diseases] Unique frequencies of HFE gene variants in Roma/Gypsies. Prevalence of 845G>A HFE mutation in Slavic populations: an east-west linear gradient in South Slavs

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