Increasing Fetal Hemoglobin may be the Key to Help People With Sickle Cell Disease and Thalassemia

An important signaling protein that regulates the production of hemoglobin was discovered. Blocking this protein can increase fetal hemoglobin production and deliver therapeutic benefits to Sickle Cell Disease (SCD) and Beta-Thalassemia.

from Medindia Health News https://ift.tt/2OyfrxZ