Open AccessP1521: 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) -
Rivella S.,
Chappell M.,
Jarocha D.,
Breda L.,
Ghiaccio V.,
Fedorky M.,
Triebwasser M.,
Guerra A.,
Gollomp K.,
Teawtrakul N.,
Glentis S.,
Kattamis A.,
Abdulmalik O.
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.hs9.0000848940.29840.9b
Subject(s) - hydrops fetalis , bone marrow , immunology , transplantation , fetal hemoglobin , thalassemia , biology , medicine , microbiology and biotechnology , fetus , genetics , pregnancy