Samuel E. Lux u. a.: Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8. In: Nature. 345, Nr. 6277, 1990, S. 736–739., doi:10.1038/345736a0, PMID 2141669.
V. Bennett, P. J. Stenbuck: Identification and partial purification of ankyrin, the high affinity membrane attachment site for human erythrocyte spectrin. In: Journal of Biological Chemistry. 254, Nr. 7, 1979, S. 2533–2541, doi:10.1016/j.bbamem.2013.09.014, PMID 372182.
Manuel A. R. Ferreira u. a.: Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. In: Nature Genetics. 40, Nr. 9, 2008, S. 1056–1058, doi:10.1038/ng.209, PMID 18711365, PMC 2703780 (freier Volltext).
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V. Bennett, P. J. Stenbuck: Identification and partial purification of ankyrin, the high affinity membrane attachment site for human erythrocyte spectrin. In: Journal of Biological Chemistry. 254, Nr. 7, 1979, S. 2533–2541, PMID 372182.
Samuel E. Lux u. a.: Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8. In: Nature. 345, Nr. 6277, 1990, S. 736–739., doi:10.1038/345736a0, PMID 2141669.
V. Bennett, P. J. Stenbuck: Identification and partial purification of ankyrin, the high affinity membrane attachment site for human erythrocyte spectrin. In: Journal of Biological Chemistry. 254, Nr. 7, 1979, S. 2533–2541, doi:10.1016/j.bbamem.2013.09.014, PMID 372182.
Manuel A. R. Ferreira u. a.: Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. In: Nature Genetics. 40, Nr. 9, 2008, S. 1056–1058, doi:10.1038/ng.209, PMID 18711365, PMC 2703780 (freier Volltext).