HFE mutations in patients with hereditary haemochromatosis in Sweden.

To determine the frequency of mutations (C282Y and H63D) in a newly identified gene HFE in patients with hereditary haemochromatosis (HH) in Sweden. DESIGN: Molecular genetic analyses of the HFE gene (polymerase chain reaction (PCR) followed by enzyme restriction) were performed in genomic DNA from...

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Detalhes bibliográficos
Autor principal: Cardoso, Elsa M. (author)
Outros Autores: Stal, Per (author), Hagen, Karin (author), Cabeda, José M. (author)
Formato: article
Idioma:eng
Publicado em: 2016
Assuntos:
genotype
haemochromatosis
HFE
inherited disorders
iron
Texto completo:http://hdl.handle.net/10314/3510
País:Portugal
Oai:oai:bdigital.ipg.pt:10314/3510

Texto Completo

http://hdl.handle.net/10314/3510

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