Hemojuvelin and Hepcidin Genes Sequencing in Brazilian Patients with Primary Iron Overload-Reference-Cited by-同舟云学术

Hemojuvelin and Hepcidin Genes Sequencing in Brazilian Patients with Primary Iron Overload

Published:2010-12 Issue:6 Volume:14 Page:803-806
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

de Lima Santos Paulo Caleb Júnior¹,Pereira Alexandre C.²,Cançado Rodolfo D.³,Schettert Isolmar T.²⁴,Hirata Rosario D.C.¹,Hirata Mario H.¹,Figueiredo Maria Stella⁵,Chiattone Carlos S.³,Krieger Jose E.²,Guerra-Shinohara Elvira M.¹

Affiliation:

1. Department of Clinical Chemistry and Toxicology, School of Pharmaceutical Sciences, University of Sao Paulo, Sao Paulo, Brazil.

2. Laboratory of Genetics and Molecular Cardiology, Heart Institute, University of Sao Paulo Medical School, Sao Paulo, Brazil.

3. Department of Hematology and Oncology of Santa Casa School of Medicine/Santa Casa Blood Center of Sao Paulo, Sao Paulo, Brazil.

4. Novo Atibaia Hospital, Sao Paulo, Brazil.

5. Department of Hematology and Hemotherapy, EPM/UNIFESP, Sao Paulo, Brazil.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2010.0056

Reference33 articles.

1. Nonexpressing Homozygotes for C282Y Hemochromatosis: Minority or Majority of Cases?

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

3. The Evaluation of Hyperferritinemia: An Updated Strategy Based on Advances in Detecting Genetic Abnormalities

4. Iron-Overload–Related Disease inHFEHereditary Hemochromatosis

5. Mutations in HAMP and HJV genes and their impact on expression of clinical hemochromatosis in a cohort of 100 Spanish patients homozygous for the C282Y mutation of HFE gene

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