Coinheritance of PIEZO1 variants and multi‐locus red blood cell defects account for the symptomatic phenotype in beta‐thalassemia carriers.
- Resource Type
- Article
- Source
- American Journal of Hematology; Jun2023, Vol. 98 Issue 6, pE130-E133, 4p
- Subject
- Language
- ISSN
- 03618609