- Tytuł:
- Next generation sequencing (NGS) interest in deciphering erythrocyte molecular defects' association in red cell disorders: Clinical and erythrocyte phenotypes of patients with mutations inheritance in PIEZO1, Spectrin ß1, RhAG and SLC4A1
- Autorzy:
- Źródło:
- In Blood Cells, Molecules and Diseases November 2023 103
Czasopismo naukowe