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2022 | 1 |
2023 | 1 |
2024 | 0 |
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Whole exome sequencing identifies a novel SPTB frameshift mutation causing hereditary spherocytosis in the Chinese population.
Ann Hematol. 2022 Oct;101(10):2355-2357. doi: 10.1007/s00277-022-04900-0. Epub 2022 Jun 21.
Ann Hematol. 2022.
PMID: 35726106
No abstract available.
Hematopoietic cell transplantation for congenital dyserythropoietic anemia IV caused by compound heterozygous KLF1 mutations.
Yang K, Nie W, Huang Q, Liao G, Xiao J, Yin X.
Yang K, et al.
Ann Hematol. 2023 Jun;102(6):1621-1624. doi: 10.1007/s00277-023-05175-9. Epub 2023 Mar 31.
Ann Hematol. 2023.
PMID: 37002443
No abstract available.
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