학술논문
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
Document Type
Article
Author
Source
In: Blood Cells, Molecules, and Diseases . (Blood Cells, Molecules, and Diseases, November 2023, 103)
Subject
Language
English
ISSN
10960961
10799796
10799796