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7. Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis. Eber SW; Gonzalez JM; Lux ML; Scarpa AL; Tse WT; Dornwell M; Herbers J; Kugler W; Ozcan R; Pekrun A; Gallagher PG; Schröter W; Forget BG; Lux SE Nat Genet; 1996 Jun; 13(2):214-8. PubMed ID: 8640229 [TBL] [Abstract][Full Text] [Related]
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12. Low frequency of ankyrin mutations in hereditary spherocytosis: identification of three novel mutations. Leite RC; Basseres DS; Ferreira JS; Alberto FL; Costa FF; Saad ST Hum Mutat; 2000 Dec; 16(6):529. PubMed ID: 11102985 [TBL] [Abstract][Full Text] [Related]
13. Functional analysis of a novel cis-acting regulatory region within the human ankyrin gene (ANK-1) promoter. Laflamme K; Owen AN; Devlin EE; Yang MQ; Wong C; Steiner LA; Garrett LJ; Elnitski L; Gallagher PG; Bodine DM Mol Cell Biol; 2010 Jul; 30(14):3493-502. PubMed ID: 20479128 [TBL] [Abstract][Full Text] [Related]
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20. High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis. Miraglia del Giudice E; Francese M; Nobili B; Morlé L; Cutillo S; Delaunay J; Perrotta S J Pediatr; 1998 Jan; 132(1):117-20. PubMed ID: 9470011 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]