HFE mutations in patients with hereditary haemochromatosis in Sweden

OBJECTIVE: 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 genomi...

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Detalhes bibliográficos
Autor principal: Cardoso, E. (author)
Outros Autores: Stal, P. (author), Hagen, K. (author), Cabeda, J. (author), Esin, S. (author), Sousa, M. (author), Hultcrantz, R. (author)
Formato: article
Idioma:eng
Publicado em: 2010
Texto completo:http://hdl.handle.net/10400.16/444
País:Portugal
Oai:oai:repositorio.chporto.pt:10400.16/444

Texto Completo

http://hdl.handle.net/10400.16/444

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