Open AccessP1475: THE ROLE OF BCL11A AND HBS1L‐MYB SINGLE NUCLEOTIDE POLYMORPHISMS IN EGYPTIAN SICKLE CELL DISEASE PATIENTS
Author(s) -
El Maraashly A.
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.hs9.0000848756.93590.28
Subject(s) - fetal hemoglobin , single nucleotide polymorphism , genotyping , disease , medicine , biology , sickle cell anemia , haplotype , genotype , immunology , genetics , gene , fetus , pregnancy