Analysis of HFE Genes C282Y, H63D, and S65D in Patients With Hyperferritinemia From Northeastern Brazil

BACKGROUND: Hereditary hemochromatosis (HH) is a genetic disease caused by the high absorption and deposition of iron in several organs. This accumulation results in several clinical complications such as cirrhosis, arthritis, cardiopathies, diabetes, sexual disorders, and skin darkening. The H63D a...

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Bibliografiset tiedot
Julkaisussa:J Clin Lab Anal
Päätekijät: Leão, Gioconda Dias Rodrigues, Freire, Juliana Mendonça, Cunha Fernandes, Andrea Luciana Araújo, Moura de Oliveira, Taissa Maria, Leão, Nilma Dias, Gil, Erica Aires, de Vasconcelos, Roberto Chaves, Azevedo, João Paulo da Silva, de Farias Sales, Valéria Soraya, de Araújo Moura Lemos, Telma Maria, Leão, Marcos Dias, do Nascimento, Francisco Fernandes, Maciel, James Farley Rafael, de Freitas, Rodrigo Villar, de Souza Paiva, Aldair, Cavalcanti, Geraldo Barroso
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: John Wiley and Sons Inc. 2014
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Original Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6807581/
https://ncbi.nlm.nih.gov/pubmed/24395214
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.21663
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