Simultaneous detection of HFE C282Y, H63D and S65C mutations associated with type 1 haemochromatosis using a multiplex luminex bead assay
Author:
Publisher
Wiley
Subject
Genetics,Biochemistry,Immunology,General Medicine,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0039.2011.01736.x/fullpdf
Reference42 articles.
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3. Hereditary hemochromatosis - a new look at an old disease.;Pietrangelo;N Engl J Med,2004
4. Non-HFE hemochromatosis.;Pietrangelo;Semin Liver Dis,2005
5. Hereditary hemochromatosis: pathogenesis, diagnosis, and treatment.;Pietrangelo;Gastroenterology,2010
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2. Multiplex Allele-Specific PCR for Simultaneous Detection of H63D and C282Y HFE Mutations in Hereditary Hemochromatosis;The Journal of Applied Laboratory Medicine;2018-07-01
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