Transferrin Receptor-2 (TFR2) Mutation Y250X in Alabama Caucasian and African American Subjects with and without Primary Iron Overload

By Barton E.H.   West P.A.   Rivers C.A.   Barton J.C.   Acton R.T.  

Blood Cells, Molecules, and Diseases, Vol. 27, Iss. 1, 2001-01 ,pp. : 279-284

Academic Press

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Transferrin Receptor Mutation Analysis in Hereditary Hemochromatosis Patients

By Tsuchihashi Z.   Hansen S.L.   Quintana L.   Kronmal G.S.   Mapa F.A.   Feder J.N.   Motulsky R.A.K.G.  

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Transferrin Receptor-2 Gene and Non-C282Y Homozygous Patients with Hemochromatosis

By Aguilar-Martinez P.   Esculié-Coste C.   Bismuth M.   Giansily-Blaizot M.   Larrey D.   Schved J-F.  

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Commentary: Mutations of Transferrin Receptor 2 (Trf-2) and Iron Storage Disease

By Beutler E.  

Blood Cells, Molecules, and Diseases, Vol. 27, Iss. 1, 2001-01 ,pp. : 294-295

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Soluble transferrin receptor and sTfR-F index for assessing concurrent iron deficiency in patients with chronic renal failure

By Choi Jong  

Annals of Hematology, Vol. 87, Iss. 7, 2008-07 ,pp. : 575-576

Springer Publishing Company

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