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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Bibliographic Details
Main Author: Cardoso, Elsa M. (author)
Other Authors: Stal, Per (author), Hagen, Karin (author), Cabeda, José M. (author)
Format: article
Language:eng
Published: 2016
Subjects:
genotype
haemochromatosis
HFE
inherited disorders
iron
Online Access:http://hdl.handle.net/10314/3510
Country:Portugal
Oai:oai:bdigital.ipg.pt:10314/3510

Internet

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

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