MOLECULAR CHARACTERIZATION. MOLECULAR CHARACTERIZATION OF MUTATIONS IN GENES ENCODING RBC MEMBRANE PROTEINS IN RED CELL MEMBRANE DISORDERS
收藏NIAID Data Ecosystem2026-05-02 收录
下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJEB76249
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资源简介：
Hereditary spherocytosis (HS) is the most prevalent form of congenital hemolytic anemia, being caused by genetic mutations in genes encoding cytoskeletal proteins that maintain structural red blood cell membrane stability. Mutations in the ANK1 and SPTB genes are the most common causes
创建时间：
2024-06-04
