Clinical manifestations of 17 Chinese children with hereditary spherocytosis caused by novel mutations of the ANK1 gene and phenotypic analysis
Article in Frontiers in Genetics (February 2023)
The most recent citing publications are shown below. View all 3 publications that cite this research output on Dimensions.
Novel SPTB frameshift mutation in a Chinese neonatal case of hereditary spherocytosis type 2: A case report
Article in Experimental and Therapeutic Medicine (July 2022)
A Novel ANK1 Mutation in a Neonatal Hereditary Spherocytosis Case: Diagnostic Challenges and Familial Genetic Analysis
Article in Acta Haematologica (July 2022)