TY  - JOUR
AU  - Ropero, Paloma
AU  - Peral, Miriam
AU  - Sánchez Martínez, Luis Javier
AU  - Rochas, Sara
AU  - Gómez Álvarez, Miguel
AU  - Nieto, Jorge M.
AU  - González, Fernando A.
AU  - Villegas Martínez, Ana
AU  - Benavente, Celina
PY  - 2025
DO  - 10.3389/fmed.2025.1347026
SN  - 2296-858X
UR  - https://hdl.handle.net/20.500.14352/119209
T2  - Frontiers in Medicine
AB  - Objective/Background. Sickle cell disease (SCD) is a monogenic disease with a highly variable phenotype depending on the amount of fetal hemoglobin (HbF), the main modulator. Variation of HbF levels among patients is genetically regulated. HbF...
LA  - eng
M2  - 1
PB  - Frontiers Media
KW  - Sickle cell disease
KW  - Cluster haplotypes β
KW  - XmnI
KW  - BCL11A
KW  - HBS1L-MYB
KW  - Fetal hemoglobin
TI  - Phenotype of sickle cell disease. Correlation of haplotypes and polymorphisms in cluster β, BCL11A, and HBS1L−MYB. Pilot study
TY  - journal article
VL  - 12
ER  -