Fig. 3From: 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 This frame shift mutation (c.1000delA) is located in the membrane binding domain of ANK1, occurring at 334 codon (p.I334Sfs*6)Back to article page