Coinheritance of PIEZO1 variants and multi-locus red blood cell defects account for the symptomatic phenotype in beta-thalassemia carriers.
Valeria Maria PintoRoberta RussoSabrina QuintinoBarbara Eleni RosatoRoberta MarraFederica Del GiudiceMassimo MogniMassimo MaffeiAchille IolasconGian Luca ForniImmacolata AndolfoPublished in: American journal of hematology (2023)