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Marked microcytosis and increased transferrin saturation: Think about variants in SLC11A2 (DMT1)
by
Raynor, Alexandre
,
Peoc'h, Katell
,
Boi, Camille
,
Manceau, Hana
,
Pissard, Serge
,
Diallo, Karim
,
Kannengiesser, Caroline
,
Rohrlich, Pierre
Published in
Blood cells, molecules, & diseases
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Severe iron overload in a woman with homeostatic iron regulator (HFE) and a novel 5ʹ‐aminolevulinate synthase 2 (ALAS2) mutations: interactions of multiple genetic determinants
by
Gennes, Christian
,
Lamoril, Jérôme
,
Borgel, Adrien
,
Boi, Camille
,
Yao, Raphael
,
Boileau, Catherine
,
Tchernitchko, Dimitri
Published in
British journal of haematology
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Severe iron overload in a woman with homeostatic iron regulator (HFE) and a novel 5'-aminolevulinate synthase 2 (ALAS2) mutations: interactions of multiple genetic determinants
by
de Gennes, Christian
,
Lamoril, Jérôme
,
Borgel, Adrien
,
Boi, Camille
,
Yao, Raphael
,
Boileau, Catherine
,
Tchernitchko, Dimitri
Published in
British journal of haematology
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Blood Cells, Molecules, & Diseases
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British Journal Of Haematology
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Female
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Hematology
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Humans
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Iron
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5-Aminolevulinate Synthetase - Chemistry
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5-Aminolevulinate Synthetase - Genetics
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5ʹ‐Aminolevulinate Synthase 2
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Adult
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Anemia
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Anemia, Hypochromic - Genetics
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Biomarkers
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Biopsy
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Cation Transport Proteins - Genetics
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Dmt1
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Genetic Association Studies
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Genetic Predisposition To Disease
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Haemochromatosis
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Hemochromatosis Protein - Chemistry
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Hemochromatosis Protein - Genetics
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Homeostatic Iron Regulator
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Sciencedirect (Elsevier)
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Sciencedirect Freedom Collection
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