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
出版年份 2023 全文链接
标题
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
作者
关键词
-
出版物
BLOOD CELLS MOLECULES AND DISEASES
Volume 103, Issue -, Pages 102780
出版商
Elsevier BV
发表日期
2023-07-20
DOI
10.1016/j.bcmd.2023.102780
参考文献
相关参考文献
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