The origin and spread of the HFE-C282Y haemochromatosis mutation
- 29 July 2004
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 115 (4), 269-279
- https://doi.org/10.1007/s00439-004-1152-4
Abstract
No abstract availableKeywords
This publication has 71 references indexed in Scilit:
- Phenylketonuria mutations in EuropeHuman Mutation, 2003
- A role for overdominant selection in phenylketonuria? Evidence from molecular dataHuman Mutation, 2003
- Genetic haemochromatosis: genes and mutations associated with iron loadingBest Practice & Research Clinical Haematology, 2002
- Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USAThe Lancet, 2002
- HLA class I (A, B) and II (DR, DQ) Gene and Haplotype Frequencies in Blood Donors from WalesExperimental and Clinical Immunogenetics, 1998
- Phenylketonuria and the peoples of Northern IrelandHuman Genetics, 1997
- New polymorphic microsatellite markers place the haemochromatosis gene telomeric to D6S105Human Molecular Genetics, 1995
- Prevalence of abnormal iron studies in heterozygotes for hereditary hemochromatosis: An analysis of 255 heterozygotesAmerican Journal of Hematology, 1994
- Genetics of HemochromatosisNew England Journal of Medicine, 1979
- The hitch-hiking effect of a favourable geneGenetics Research, 1974