Identification of a De Novoc.1000delA ANK1 mutation associated to hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice-case reports and review of the literature

Overview of attention for article published in BMC Medical Genomics, March 2021

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Identification of a De Novoc.1000delA ANK1 mutation associated to hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice-case reports and review of the literature https://t.co/4eETZ8GiPF https://t.co/UWTccPk8TM

11 Mar 2021

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