P1521: A SEVERE MOUSE MODEL OF ALPHA-THALASSEMIA SHOWS ABNORMAL IRON METABOLISM, ERYTHROPOIESIS AND COAGULATION, AND CAN BE RESCUED BY A NOVEL GENE THERAPY APPROACH

• S. Rivella,
• M. Chappell,
• D. Jarocha,
• L. Breda,
• V. Ghiaccio,
• M. Fedorky,
• M. Triebwasser,
• A. Guerra,
• K. Gollomp,
• N. Teawtrakul,
• S. Glentis,
• A. Kattamis,
• O. Abdulmalik

Affiliations

S. Rivella

1 Pediatrics, Children’s Hospital of Philadelphia, Philadelphia, United States of America

M. Chappell

1 Pediatrics, Children’s Hospital of Philadelphia, Philadelphia, United States of America

D. Jarocha

1 Pediatrics, Children’s Hospital of Philadelphia, Philadelphia, United States of America

L. Breda

1 Pediatrics, Children’s Hospital of Philadelphia, Philadelphia, United States of America

V. Ghiaccio

1 Pediatrics, Children’s Hospital of Philadelphia, Philadelphia, United States of America

M. Fedorky

1 Pediatrics, Children’s Hospital of Philadelphia, Philadelphia, United States of America

M. Triebwasser

1 Pediatrics, Children’s Hospital of Philadelphia, Philadelphia, United States of America

A. Guerra

1 Pediatrics, Children’s Hospital of Philadelphia, Philadelphia, United States of America

K. Gollomp

1 Pediatrics, Children’s Hospital of Philadelphia, Philadelphia, United States of America

N. Teawtrakul

2 Internal Medicine, Khon Kaen University, Khon Kaen, Thailand

S. Glentis

3 Pediatrics, University of Athens, Athens, Greece

A. Kattamis

3 Pediatrics, University of Athens, Athens, Greece

O. Abdulmalik

1 Pediatrics, Children’s Hospital of Philadelphia, Philadelphia, United States of America