Influence of beta-cluster haplotypes, alpha-gene status and UGTA1 polymorphism on clinical and hematological data in sickle-cell disease children from French Guiana.

Narcisse ElengaEmma Cuadro-AlvarezElise MartinFalucar NjuieyonAntoine DefoChimène Maniassom

Published in: PloS one (2020)

Prospective studies with greater statistical power would provide more knowledge on the relationship between UGT1A1 mutations and the clinical and hematological manifestations of SCA.

Keyphrases

sickle cell disease
healthcare
young adults
gene expression
big data
dna methylation
transcription factor