Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleA de novo ankyrin mutation (ANK1 Q109X) causing severe hereditary spherocytosis from preterm neonatal period.AuthorsLiu, Sha; Jiang, Hua; Huang, Lv-Yin; Li, Dong-ZhiSubjectsGENETIC mutation; HEREDITARY spherocytosis; ANKYRINSPublicationAnnals of Hematology, 2017, Vol 96, Issue 6, p1067ISSN0939-5555Publication typecase studyDOI10.1007/s00277-017-2966-1