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Homozygosity for the hyperunstable hemoglobin variant Hb Agrinio ( HBA2 :c. 89T >C) leads to severe antenatal anemia: Eight new cases in three families
Author(s) -
Szepetowski Sarah,
Berger Claire,
Joly Philippe,
BaronJoly Sandrine,
Huguenin Yoann,
Cantais Aurélie,
Brun Sophie,
Ged Cécile,
Badens Catherine,
Thuret Isabelle,
GiansilyBlaizot Muriel,
Pissard Serge,
AguilarMartinez Patricia
Publication year - 2022
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.26687
Subject(s) - hydrops fetalis , compound heterozygosity , thalassemia , ineffective erythropoiesis , hemolytic anemia , genetics , alpha thalassemia , anemia , biology , medicine , microbiology and biotechnology , allele , gene , genotype , erythropoiesis , immunology , fetus , pregnancy

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