Prevalence of the C282Y, H63D, and S65C Mutations of theHFEGene in 1,146 Newborns from a Region of Northern Spain-Reference-Cited by-同舟云学术

Prevalence of the C282Y, H63D, and S65C Mutations of theHFEGene in 1,146 Newborns from a Region of Northern Spain

Published:2004-12 Issue:4 Volume:8 Page:407-410
ISSN:1090-6576
Container-title:Genetic Testing
language:en
Short-container-title:Genetic Testing

Author:

Altes Albert¹,Ruiz Angels¹,Barceló M Jesus²,Remacha Angel Francisco²,Puig Teresa²,Maya Antonio José³,Castell Conxa⁴,Amate Jose M⁵,Saz Zuleika⁶,Baiget Montserrat²

Affiliation:

1. Hematology Department, Hospital de l'Esperit Sant, Santa Coloma de Gramenet, Barcelona, Spain 08923.

2. Genetics, Hematology and Epidemiology Departments, Hospital de Sant Pau, Barcelona, Spain 08025.

3. Clinical Biochemistry Institute, Barcelona, Spain 08028.

4. Public Health Department, Generalitat de Catalunya, Barcelona, Spain 08028.

5. Instituto de Salud Carlos III, Madrid, Spain 28029.

6. nstituto de Salud Carlos III, Madrid, Spain 28029.

Publisher

Mary Ann Liebert Inc

Subject

Genetics (clinical)

Link

http://www.liebertpub.com/doi/pdf/10.1089/gte.2004.8.407

Reference23 articles.

1. EASL International Consensus Conference on Haemochromatosis

2. Clinical consequences of iron overload in hemochromatosis homozygotes

3. Prevalence of HFE mutations in people from North Africa living in southern France

4. Frequency of the HFE C282Y and H63D mutations in distinct ethnic groups living in Spain.

5. The HFE Cys282Tyr mutation as a necessary but not sufficient cause of clinical hereditary hemochromatosis

Cited by 32 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Association of mutations in hemochromatosis genes with clinical severity of calcium pyrophosphate arthritis;Exploration of Musculoskeletal Diseases;2023-10-31

2. Variants in PCSK7, PNPLA3 and TM6SF2 are risk factors for the development of cirrhosis in hereditary haemochromatosis;Alimentary Pharmacology & Therapeutics;2021-02-10

3. Serum hepcidin levels, iron status, and HFE gene alterations during the first year of life in healthy Spanish infants;Annals of Hematology;2018-02-05

4. Quality of life utility values for hereditary haemochromatosis in Australia;Health and Quality of Life Outcomes;2016-02-29

5. HFE gene: Structure, function, mutations, and associated iron abnormalities;Gene;2015-12