Associated Papers
Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum.
More TA et al.
Molecular Genetics and Genomics : Mgg, 2023
Clinical and genetic diagnosis of thirteen Japanese patients with hereditary spherocytosis.
Yamamoto KS et al.
Human Genome Variation, 2022
Select a paper to view details