Open AccessS104: A SEVERE MOUSE MODEL OF ALPHA‐THALASSEMIA SHOWS ABNORMAL IRON METABOLISM, ERYTHROPOIESIS AND COAGULATION, AND CAN BE RESCUED BY A NOVEL GENE THERAPY APPROACH
Author(s) -
Chappell M,
Breda L,
Guerra A,
Ghiaccio V,
Fedorky M,
Jarocha D,
Gollomp K,
Teawtrakul N,
Glentis S,
Kattamis A,
Rivella S
Publication year - 2022
Publication title -
hemasphere
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.677
H-Index - 11
ISSN - 2572-9241
DOI - 10.1097/01.hs9.0000821384.16305.a3
Subject(s) - hydrops fetalis , bone marrow , immunology , fetal hemoglobin , transplantation , thalassemia , medicine , biology , microbiology and biotechnology , fetus , genetics , pregnancy