The studies of the HFE mutations: H63D and C282Y in North African populations have revealed the extreme rarity or even the absence of the C282Y mutation. We have examined 200 chromosomes (100 Libyan people live in Benghazi) for the presence of the two HFE mutations by PCR-RFLP analysis by using PCR conditions used to amplify both Autosomal and Y chromosomal STRs. We have found that the allele frequencies are, respectively, 17% for the H63D and 0% for the C282Y. These results are consistent with the worldwide spread of the H63D mutation and the north European restriction of the C282Y
SummaryGenetic hemochromatosis (GH) is believed to be a disease restricted to those of European ance...
Hereditary haemochromatosis is an autosomal recessive disorder of iron regulation that results in a...
Purpose: The prevalence of HFE-related hereditary hemochromatosis (HH) among European populations h...
The frequencies of the hereditary hemochromatosis gene (HFE) mutations C282Y and H63D vary between d...
International audienceThe occurrence of the C282Y and H63D mutations of the HFE gene, responsible fo...
Background: Hereditary hemochromatosis (HH) is an autosomal recessive disorder of iron metabolism ca...
International audienceThe distribution of HFE mutations was studied in patients from the French Basq...
A Celtic origin for hemochromatosis, a common genetic iron metabolism disorder, has been postulated ...
Hereditary hemochromatosis (HH) is a common autosomal recessive disorder causing inappropriate dieta...
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,...
Hereditary haemochromatosis is an autosomal recessive disorder of iron regulation that results in ab...
Objectives: To determine the frequency of hereditary hemochromatosis gene mutations, C282Y and H63D,...
The hemochromatosis gene, HFE, is located on chromosome 6 in close proximity to the HLA-A locus. Mos...
Objective. To determine the frequency of mutations (C282Y and H63D) in a newly identified gene HFE i...
SummaryGenetic hemochromatosis (GH) is believed to be a disease restricted to those of European ance...
Hereditary haemochromatosis is an autosomal recessive disorder of iron regulation that results in a...
Purpose: The prevalence of HFE-related hereditary hemochromatosis (HH) among European populations h...
The frequencies of the hereditary hemochromatosis gene (HFE) mutations C282Y and H63D vary between d...
International audienceThe occurrence of the C282Y and H63D mutations of the HFE gene, responsible fo...
Background: Hereditary hemochromatosis (HH) is an autosomal recessive disorder of iron metabolism ca...
International audienceThe distribution of HFE mutations was studied in patients from the French Basq...
A Celtic origin for hemochromatosis, a common genetic iron metabolism disorder, has been postulated ...
Hereditary hemochromatosis (HH) is a common autosomal recessive disorder causing inappropriate dieta...
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,...
Hereditary haemochromatosis is an autosomal recessive disorder of iron regulation that results in ab...
Objectives: To determine the frequency of hereditary hemochromatosis gene mutations, C282Y and H63D,...
The hemochromatosis gene, HFE, is located on chromosome 6 in close proximity to the HLA-A locus. Mos...
Objective. To determine the frequency of mutations (C282Y and H63D) in a newly identified gene HFE i...
SummaryGenetic hemochromatosis (GH) is believed to be a disease restricted to those of European ance...
Hereditary haemochromatosis is an autosomal recessive disorder of iron regulation that results in a...
Purpose: The prevalence of HFE-related hereditary hemochromatosis (HH) among European populations h...