Background: Iron-refractory iron deficiency anaemia (IRIDA) is a rare disorder which was linked to mutations in two genes (SLC11A2 and TMPRSS6). Common polymorphisms within these genes were associated with serum iron levels. We identified a family of Serbian origin with asymptomatic non-consanguineous parents with three of four children presenting with IRIDA not responding to oral but to intravenous iron supplementation. After excluding all known causes responsible for iron deficiency anaemia we searched for mutations in SLC11A2 and TMPRSS6 that could explain the severe anaemia in these children. Methodology/Results: We sequenced the exons and exon–intron boundaries of SLC11A2 and TMPRSS6 in all six family members. Thereby, we found seven k...
Iron-refractory iron deficiency anemia (IRIDA) is a rare autosomal recessive anemia usually unrespon...
Contains fulltext : 137523.pdf (publisher's version ) (Open Access)Variation in bo...
Iron refractory iron deficiency anemia (IRIDA) is an autosomal recessive ferropenic anemia. Its hypo...
BACKGROUND: Iron-refractory iron deficiency anaemia (IRIDA) is a rare disorder which was linked to m...
BACKGROUND: Iron-refractory iron deficiency anaemia (IRIDA) is a rare disorder which was linked to m...
<div><h3>Background</h3><p>Iron-refractory iron deficiency anaemia (IRIDA) is a rare disorder which ...
Objective: Iron-refractory iron-deficiency anaemia (IRIDA) is a rare autosomal-recessive disease cha...
Iron-refractory iron deficiency anemia (IRIDA) is a rare autosomal recessive anemia often unresponsi...
Male subjects with iron deficiency from the general population were examined for polymorphisms or sp...
Contains fulltext : 89715.pdf (publisher's version ) (Closed access)Male subjects ...
Contains fulltext : 172863.pdf (Publisher’s version ) (Open Access)TMPRSS6 variant...
Iron-refractory iron-deficiency anemia (IRIDA) is a rare autosomal-recessive disorder characterized ...
Iron refractory iron deficiency anemia (IRIDA) is a rare hereditary disease caused by mutations in T...
Matriptase-2 (Tmprss6), a type II transmembrane serine protease, has an essential role in iron homoe...
TMPRSS6 variants that affect protein function result in impaired matriptase-2 function and consequen...
Iron-refractory iron deficiency anemia (IRIDA) is a rare autosomal recessive anemia usually unrespon...
Contains fulltext : 137523.pdf (publisher's version ) (Open Access)Variation in bo...
Iron refractory iron deficiency anemia (IRIDA) is an autosomal recessive ferropenic anemia. Its hypo...
BACKGROUND: Iron-refractory iron deficiency anaemia (IRIDA) is a rare disorder which was linked to m...
BACKGROUND: Iron-refractory iron deficiency anaemia (IRIDA) is a rare disorder which was linked to m...
<div><h3>Background</h3><p>Iron-refractory iron deficiency anaemia (IRIDA) is a rare disorder which ...
Objective: Iron-refractory iron-deficiency anaemia (IRIDA) is a rare autosomal-recessive disease cha...
Iron-refractory iron deficiency anemia (IRIDA) is a rare autosomal recessive anemia often unresponsi...
Male subjects with iron deficiency from the general population were examined for polymorphisms or sp...
Contains fulltext : 89715.pdf (publisher's version ) (Closed access)Male subjects ...
Contains fulltext : 172863.pdf (Publisher’s version ) (Open Access)TMPRSS6 variant...
Iron-refractory iron-deficiency anemia (IRIDA) is a rare autosomal-recessive disorder characterized ...
Iron refractory iron deficiency anemia (IRIDA) is a rare hereditary disease caused by mutations in T...
Matriptase-2 (Tmprss6), a type II transmembrane serine protease, has an essential role in iron homoe...
TMPRSS6 variants that affect protein function result in impaired matriptase-2 function and consequen...
Iron-refractory iron deficiency anemia (IRIDA) is a rare autosomal recessive anemia usually unrespon...
Contains fulltext : 137523.pdf (publisher's version ) (Open Access)Variation in bo...
Iron refractory iron deficiency anemia (IRIDA) is an autosomal recessive ferropenic anemia. Its hypo...