Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Combined spectrin and ankyrin deficiency is common in autosomal dominant hereditary spherocytosis.

Combined spectrin and ankyrin deficiency is common in autosomal dominant hereditary spherocytosis. Blood. 1993 Nov 15; 82(10):2953-60.

View in: PubMed

Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.