The role of hemoglobin F in sickle cell disease complications: a descriptive secondary analysis
Year: 2025
Type: article
Abstract: = .038). Further research is warranted to investigate whether other treatments for SCD produce similar results and whether this effect is representative of other large patient populations with SCD.
Authors: Heath Aston, Elexis Price, Elena Wernecke, Emma Hazenberg, Daniel Herrera, Siera Gollan, Hongyan Xu, Girindra Raval, Abdullah Kutlar
Institution: Augusta University
Language: English
Subfield: Genetics
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,000
OpenAlex ID: W4415016808