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Annals of Hematology, Vol. 83, Iss. 10, 2004-10 ,pp. : 654-657

Springer Publishing Company

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A Rare Case of a Patient Heterozygous for the Hemochromatosis Mutation C282Y and Homozygous for H63D

By Lucotte G.   Champenois T.   Sémonin O.  

Blood Cells, Molecules, and Diseases, Vol. 27, Iss. 5, 2001-05 ,pp. : 892-893

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Two Novel Missense Mutations of the HFE Gene (I105T and G93R) and Identification of the S65C Mutation in Alabama Hemochromatosis Probands

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Frequency of the C282Y Mutation of Hemochromatosis in Five French Populations

By Mercier G.   Bathelier C.   Beutler G.E.  

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Pearson syndrome in an infant heterozygous for C282Y allele of HFE gene

By Kefala-Agoropoulou Kalomoira   Roilides Emmanuel   Lazaridou Anna   Karatza Eliza   Farmaki Evangelia   Tsantali Haido   Augoustides-Savvopoulou Persephone   Tsiouris John  

Hematology, Vol. 12, Iss. 6, 2007-12 ,pp. : 549-553

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