Coinheritance of PIEZO1 variants and multi-locus red blood cell defects account for the symptomatic phenotype in beta-thalassemia carriers

Am J Hematol. 2023 Jun;98(6):E130-E133. doi: 10.1002/ajh.26901. Epub 2023 Mar 17.

Abstract

Workflow of the study with some examples of the achieved results.

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Erythrocytes
  • Heterozygote
  • Humans
  • Ion Channels / genetics
  • Phenotype
  • beta-Thalassemia* / genetics

Substances

  • PIEZO1 protein, human
  • Ion Channels