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 4 publications that cite this research output on Dimensions.
A Case Report of Hereditary Spherical with ANK1 Gene Mutation and Literature Review
Article in Advances in Clinical Medicine (January 2023)
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)