A case report of congenital dyserythropoietic anemia type II with a novel SEC23B mutation and accompanied by a large segmental deletion and literature review
Preprint in Research Square (June 2024)
The most recent citing publications are shown below. View all 21 publications that cite this research output on Dimensions.
Identification of the molecular etiology in rare congenital hemolytic anemias using next‐generation sequencing with exome‐based copy number variant analysis
Article in European Journal Of Haematology (March 2024)
Current Status of Molecular Diagnosis of Hereditary Hemolytic Anemia in Korea
Article in Journal of Korean Medical Science (January 2024)