Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis

Stefan W. Eber, Jennifer M. Gonzalez, Marcia L. Lux, Alphonse L. Scarpa, William T. Tse, Marion Dornwell, Jutta Herbers, Wilfried Kugler, Refik Özcan, Arnulf Pekrun, Patrick G. Gallagher, Werner Schröter, Bernard G. Forget, Samuel E. Lux*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

173 Scopus citations

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Medicine & Life Sciences