Glyceronephosphate O-acyltransferase (GNPAT) p.D519G (rs11558492) was identified as a genetic modifier correlated with more severe iron overload in hemochromatosis through whole-exome sequencing of HFE p.C282Y homozygotes with extreme iron phenotypes. We studied the prevalence of p.D519G in HFE p.C282Y/p.H63D compound heterozygotes, a genotype associated with iron overload in some patients. Cases were Australian participants with elevated serum ferritin (SF) levels ≥300μg/L (males) and ≥200μg/L (females); subjects whose SF levels were below these cut-offs were designated as controls. Samples were genotyped for GNPAT p.D519G. We compared the allele frequency of the present subjects, with/without elevated SF, to p.D519G frequency in public da...
HFE-associated hereditary hemochromatosis (HH) is a genetic predisposition to iron overload and subs...
The ferroportin (FPN1) Q248H polymorphism has been associated with increased serum ferritin (SF) lev...
Contains fulltext : 137523.pdf (publisher's version ) (Open Access)Variation in bo...
Background. Previous studies in high and low expressors has demonstrated that a variant in the GNPAT...
To identify polymorphisms associated with variability of iron overload severity in HFE-associated he...
Background and Aim. HFE-related Hemochromatosis (HH) is characterized by marked phenotype heterogene...
BACKGROUND: GNPAT p.D519G positivity is significantly increased in HFE p.C282Y homozygotes with mark...
Both familial and sporadic porphyria cutanea tarda (PCT) are iron dependent diseases. Symptoms of PC...
Exome sequencing has identified the glyceronephosphate O-acyltransferase (GNPAT) gene as a genetic m...
Both familial and sporadic porphyria cutanea tarda (PCT) are iron dependent diseases. Symptoms of PC...
HFE-related Hemochromatosis (HH) is characterized by marked phenotype heterogeneity, probably due to...
There is emerging evidence that there are genetic modifiers of iron indices for HFE gene mutation ca...
HFE hemochromatosis is characterized by increased iron absorption and iron overload due to variants ...
The risk of hemochromatosis-related morbidity is unknown among HFE compound heterozygotes (C282Y/H63...
International audienceHereditary hemochromatosis is a common-recessive-autosomal disease characteriz...
HFE-associated hereditary hemochromatosis (HH) is a genetic predisposition to iron overload and subs...
The ferroportin (FPN1) Q248H polymorphism has been associated with increased serum ferritin (SF) lev...
Contains fulltext : 137523.pdf (publisher's version ) (Open Access)Variation in bo...
Background. Previous studies in high and low expressors has demonstrated that a variant in the GNPAT...
To identify polymorphisms associated with variability of iron overload severity in HFE-associated he...
Background and Aim. HFE-related Hemochromatosis (HH) is characterized by marked phenotype heterogene...
BACKGROUND: GNPAT p.D519G positivity is significantly increased in HFE p.C282Y homozygotes with mark...
Both familial and sporadic porphyria cutanea tarda (PCT) are iron dependent diseases. Symptoms of PC...
Exome sequencing has identified the glyceronephosphate O-acyltransferase (GNPAT) gene as a genetic m...
Both familial and sporadic porphyria cutanea tarda (PCT) are iron dependent diseases. Symptoms of PC...
HFE-related Hemochromatosis (HH) is characterized by marked phenotype heterogeneity, probably due to...
There is emerging evidence that there are genetic modifiers of iron indices for HFE gene mutation ca...
HFE hemochromatosis is characterized by increased iron absorption and iron overload due to variants ...
The risk of hemochromatosis-related morbidity is unknown among HFE compound heterozygotes (C282Y/H63...
International audienceHereditary hemochromatosis is a common-recessive-autosomal disease characteriz...
HFE-associated hereditary hemochromatosis (HH) is a genetic predisposition to iron overload and subs...
The ferroportin (FPN1) Q248H polymorphism has been associated with increased serum ferritin (SF) lev...
Contains fulltext : 137523.pdf (publisher's version ) (Open Access)Variation in bo...