Was the C282Y mutation an Irish Gaelic mutation that the Vikings helped disseminate?*
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.2010.01536.x/fullpdf
Reference45 articles.
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3. Declining prevalence of diabetes mellitus in hereditary haemochromatosis - the result of earlier diagnosis;O’Sullivan;Diabetes Res Clin Pract,2008
4. A study of 609 HLA haplotypes marking for the hemochromatosis gene;Simon;Am J Hum Genet,1987
5. The origin and spread of the HFE-C282Y haemochromatosis mutation;Distante;Hum Genet,2004
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2. Contributions of HFE polymorphisms to brain and blood iron load, and their links to cognitive and motor function in healthy adults;Neuropsychopharmacology Reports;2021-07-21
3. Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes;Hereditas;2017-12
4. Iron loading in HFE p.C282Y homozygotes found by population screening: relationships to HLA-type and T-lymphocyte subsets;Scandinavian Journal of Clinical and Laboratory Investigation;2017-07-05
5. Different distribution of the common HFE variants between western and eastern Spanish populations evidences an independent haplotype gene flow;Revista del Laboratorio Clínico;2017-04
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