Mutation of a barrier insulator in the human ankyrin-1 gene is associated with hereditary spherocytosis.
Gallagher PG; Steiner LA; Liem RI; Owen AN; Cline AP; Seidel NE; Garrett LJ; Bodine DM; The Journal Of Clinical Investigation, 2010, vol. 120, issue 12, p 4453, ISSN 15588238. ISBN 15588238.

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