<p>Patients positive for the beta-thalassemia trait were classified as “Beta-trait”, next if negative for “Beta-trait” and positive for <i>HFE</i> genotypes at risk as “HFE at risk”, and among the remaining patients those homozygous for the 736V/V TMPSS6 as “736VV”, and the rest as “none”.</p
Background and aims: Although most cases of hereditary haemochromatosis are associated with homozygo...
Contains fulltext : 137523.pdf (publisher's version ) (Open Access)Variation in bo...
The existence of multiple inherited disorders of iron metabolism suggests genetic contributions to i...
Hereditary hemochromatosis due to homozygosity for the C282Y mutation in the HFE gene product is the...
AIM: This study aimed to detect the most common HFE gene mutations (C282Y, H63D, and S56C) in Egypti...
<p>ALT: alanine aminotransferases; BMI: body mass index; CRP: C reactive protein; TS%: transferrin s...
International audienceC282Y homozygosity is necessary (but insufficient in isolation) for the onset ...
BACKGROUND: Iron is integral to many physiological processes, and variations in its levels, even wit...
There is emerging evidence that there are genetic modifiers of iron indices for HFE gene mutation ca...
Background/Aims: HFE-related haemochromatosis is a common disorder of iron metabolism. Most affected...
People with genetic haemochromatosis (GH) accumulate iron from excessive dietary absorption. In popu...
BackgroundIron is integral to many physiological processes, and variations in its levels, even withi...
Background and aims: Although most cases of hereditary haemochromatosis are associated with homozygo...
Contains fulltext : 137523.pdf (publisher's version ) (Open Access)Variation in bo...
The existence of multiple inherited disorders of iron metabolism suggests genetic contributions to i...
Hereditary hemochromatosis due to homozygosity for the C282Y mutation in the HFE gene product is the...
AIM: This study aimed to detect the most common HFE gene mutations (C282Y, H63D, and S56C) in Egypti...
<p>ALT: alanine aminotransferases; BMI: body mass index; CRP: C reactive protein; TS%: transferrin s...
International audienceC282Y homozygosity is necessary (but insufficient in isolation) for the onset ...
BACKGROUND: Iron is integral to many physiological processes, and variations in its levels, even wit...
There is emerging evidence that there are genetic modifiers of iron indices for HFE gene mutation ca...
Background/Aims: HFE-related haemochromatosis is a common disorder of iron metabolism. Most affected...
People with genetic haemochromatosis (GH) accumulate iron from excessive dietary absorption. In popu...
BackgroundIron is integral to many physiological processes, and variations in its levels, even withi...
Background and aims: Although most cases of hereditary haemochromatosis are associated with homozygo...
Contains fulltext : 137523.pdf (publisher's version ) (Open Access)Variation in bo...
The existence of multiple inherited disorders of iron metabolism suggests genetic contributions to i...