Associated Papers
A novel variant in the SPTB gene underlying hereditary spherocytosis and a literature review of previous variants.
Wang Y et al.
Bmc Medical Genomics, 2024
39135028 (PubMed )
Supplement: 12920_2024_1973_MOESM6_ESM.docx
Precise diagnosis of a hereditary spherocytosis patient with complicated hematological phenotype.
Liang G et al.
Molecular Genetics and Genomics : Mgg, 2024
Genetic and Clinical Characteristics of Patients With Hereditary Spherocytosis in Hubei Province of China.
Wang X et al.
Frontiers in Genetics, 2020
[Clinical manifestations of erythrocyte membrane protein coding gene mutations in hereditary spherocytosis].
Sun XJ et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi, 2018
Select a paper to view details