Spectrum of Ankyrin Mutations in Hereditary Spherocytosis: A Case Report and Review of the Literature

Conclusion: A novelANK1 mutation (NM_000037.3, c.2960+2T#x3e;G, intron 26) that is potentially associated with HS was identified. To date, 80ANK1 mutations have been reported to be associated with HS in humans.Acta Haematol 2018;140:77 –86

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Source: Acta Haematologica - September 18, 2018 Category: Hematology Source Type: research