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Vol. 145. Issue 1.
Pages 42-43 (July 2015)
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Vol. 145. Issue 1.
Pages 42-43 (July 2015)
Letter to the Editor
Usefulness of a diagnostic algorithm hyperferritinemia: A case report of a Spanish family with hereditary hemochromatosis and mutation in SLC40A1 gene
Utilidad de un algoritmo diagnóstico en la hiperferritinemia: presentación de una familia española con hemocromatosis hereditaria y mutación en el gen SLC40A1
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Juan Antonio Vargasa,b, Alejandro Muñoza, Begoña Samperc, Belén Bornsteinb,c,d,
Corresponding author
a Servicio de Medicina Interna, Hospital Universitario Puerta de Hierro, Majadahonda, Madrid, Spain
b Instituto de Investigación Biomédica Puerta de Hierro (IDIPHIM), Majadahonda, Madrid, Spain
c Servicio de Bioquímica, Hospital Universitario Puerta de Hierro, Majadahonda, Madrid, Spain
d Centro de Investigación Biomédica en Red en Enfermedades Raras (CIBERER), Madrid, Spain
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