Associated Papers
Genome-wide detection of human intronic AG-gain variants located between splicing branchpoints and canonical splice acceptor sites.
Zhang P et al.
Proceedings of the National Academy of Sciences of the United States of America, 2023
37931111 (PubMed )
Supplement: pnas.2314225120.sd01.xlsx › Dataset_S1._patho_AG-gain_var
Genotype-degree of hemolysis correlation in hereditary spherocytosis.
Shi Y et al.
Bmc Genomics, 2023
Exome sequencing for diagnosis of congenital hemolytic anemia.
Mansour-Hendili L et al.
Orphanet Journal of Rare Diseases, 2020
Gilbert's syndrome coexisting with hereditary spherocytosis might not be rare: Six case reports.
Kang LL et al.
World Journal of Clinical Cases, 2020
Select a paper to view details