International audienceThe distribution of HFE mutations was studied in patients from the French Basque Country with hereditary hemochromatosis (HH). The C282Y mutation was underrepresented but H63D seemed to demonstrate the highest prevalence when compared with other European countries. In addition, symptomatic HH was rarer in autochthonous Basques. This profile is interesting to consider in view of population genetics and should be associated with the search for non-HFE mutation
The hemochromatosis gene, HFE, is located on chromosome 6 in close proximity to the HLA-A locus. Mos...
Hereditary hemochromatosis (HH) is a common autosomal recessive disorder in populations of European ...
The studies of the HFE mutations: H63D and C282Y in North African populations have revealed the extr...
International audienceThe distribution of HFE mutations was studied in patients from the French Basq...
Hereditary hemochromatosis (HH) is a common autosomal recessive disorder causing inappropriate dieta...
The frequencies of the hereditary hemochromatosis gene (HFE) mutations C282Y and H63D vary between d...
Hereditary haemochromatosis is an autosomal recessive disorder of iron regulation that results in ab...
Hereditary HFE Hemochromatosis is an inherited disorder of iron metabolism that results from mutatio...
Objectives: To determine the frequency of hereditary hemochromatosis gene mutations, C282Y and H63D,...
Genetic testing for hemochromatosis may have important implications for diagnosis and screening of t...
This study aims to investigate the genotype-phenotype correlation of the hereditary hemochromatosis ...
Hereditary haemochromatosis is an autosomal recessive disorder of iron regulation that results in a...
Objectives: To determine the frequency of hereditary hemochromatosis gene mutations, C282Y and H63D,...
HFE genotyping is now firmly established as an essential diagnostic tool in the management of geneti...
Classical hereditary hemochromatosis is a recessive autosomal disease related to a systemic iron ove...
The hemochromatosis gene, HFE, is located on chromosome 6 in close proximity to the HLA-A locus. Mos...
Hereditary hemochromatosis (HH) is a common autosomal recessive disorder in populations of European ...
The studies of the HFE mutations: H63D and C282Y in North African populations have revealed the extr...
International audienceThe distribution of HFE mutations was studied in patients from the French Basq...
Hereditary hemochromatosis (HH) is a common autosomal recessive disorder causing inappropriate dieta...
The frequencies of the hereditary hemochromatosis gene (HFE) mutations C282Y and H63D vary between d...
Hereditary haemochromatosis is an autosomal recessive disorder of iron regulation that results in ab...
Hereditary HFE Hemochromatosis is an inherited disorder of iron metabolism that results from mutatio...
Objectives: To determine the frequency of hereditary hemochromatosis gene mutations, C282Y and H63D,...
Genetic testing for hemochromatosis may have important implications for diagnosis and screening of t...
This study aims to investigate the genotype-phenotype correlation of the hereditary hemochromatosis ...
Hereditary haemochromatosis is an autosomal recessive disorder of iron regulation that results in a...
Objectives: To determine the frequency of hereditary hemochromatosis gene mutations, C282Y and H63D,...
HFE genotyping is now firmly established as an essential diagnostic tool in the management of geneti...
Classical hereditary hemochromatosis is a recessive autosomal disease related to a systemic iron ove...
The hemochromatosis gene, HFE, is located on chromosome 6 in close proximity to the HLA-A locus. Mos...
Hereditary hemochromatosis (HH) is a common autosomal recessive disorder in populations of European ...
The studies of the HFE mutations: H63D and C282Y in North African populations have revealed the extr...