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Diagnostic value of targeted next‐generation sequencing in suspected hemochromatosis patients with a single copy of the HFE p.Cys282Tyr causative allele
Author(s) -
Uguen Kevin,
Scotet Virginie,
Ka Chandran,
Gourlaouen Isabelle,
L'hostis Carine,
Merour MarieChristine,
Cuppens Tania,
Ferec Claude,
Le Gac Gerald
Publication year - 2017
Publication title -
american journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.456
H-Index - 105
eISSN - 1096-8652
pISSN - 0361-8609
DOI - 10.1002/ajh.24912
Subject(s) - hemochromatosis , compound heterozygosity , hereditary hemochromatosis , allele , genetics , genotype , hamp , transferrin saturation , heterozygote advantage , phlebotomy , biology , medicine , hepcidin , gene , iron deficiency , anemia
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