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bibliographicCitation Chai S, Jiao R, Sun X, Fu P, Zhao Q, Sang M. Novel nonsense mutation p. Gln264Ter in the ANK1 confirms causative role for hereditary spherocytosis: a case report. BMC Medical Genomics. 2020 Nov 13;21(1):223. doi: 10.1186/s12881-020-01161-4.
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title Novel nonsense mutation p. Gln264Ter in the ANK1 confirms causative role for hereditary spherocytosis: a case report
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