Allogenic haematopoeitic stem cell transplant as cure for severe transfusion-dependent non-dominant hereditary spherocytosis due to homozygous SPTA1 mutation.
Subramaniam RamanathanWing RobertsPeter CareyScott MarshallGeoff ShentonMiriam Munoz-DiazTina BissRoderick SkinnerJosu De La FuenteMary SlatterSu Han LumPublished in: Pediatric blood & cancer (2022)