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publicationName Annals of Hematology
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bibliographicCitation Liu XD, Yang K, Xiao J, Huang H, Zhang XD, Huang JY. Whole exome sequencing identifies a novel SPTB frameshift mutation causing hereditary spherocytosis in the Chinese population. Ann Hematol. 2022 Oct;101(10):2355–7. doi: 10.1007/s00277-022-04900-0. PMID: 35726106.
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title Whole exome sequencing identifies a novel SPTB frameshift mutation causing hereditary spherocytosis in the Chinese population
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Total number of triples: 32.