Therapeutic gene editing strategies using CRISPR-Cas9 for the β-hemoglobinopathies
James B.Papizan
Shaina N.Porter
Akshay Sharma
Shondra M.Pruett-Miller
Keywords：sickle cell diseasesickle cell anemiafetal hemoglobinhemoglobinopathyCRISPRgene editinggenome engineering
Publication Date：2021-03-30
Online Publishing Date：2025-08-15(First online date of this platform, not the publication date of the document)
Pages：20( 115-134 )