Work

Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency.

Year: 1997

Type: article

Study design: Observational Study

Source: PubMed

DOI: 10.1182/blood.v90.1.398

Authors: H Hassoun, J N Vassiliadis, J Murray, P R Njolstad, J J Rogus, S K Ballas, F Schaffer, P Jarolim, V Brabec, J Palek

Institutions: Tufts University, St. Elizabeth's Medical Center

Language: English

Topic: Erythrocyte Function and Pathophysiology

Subfield: Physiology (medical)

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: National Heart, Lung, and Blood Institute

Awards: G1634432615, ANKYRIN MUTATIONS IN HEREDITARY SPHEROCYTOSIS, G681746002, MEMBRANE SKELETON OF NORMAL AND ABNORMAL RED CELLS

OpenAlex ID: W75318692

FWCI: 2.747

Cites: 53

Cited by: 77

Related to: 10