Work

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

Year: 1996

Type: article

Study design: Observational Study

Source: Nature Genetics

DOI: 10.1038/ng0696-214

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

Institutions: Boston Children's Hospital, Yale University, Universitätsmedizin Göttingen, Harvard University, Dana-Farber Cancer Institute

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

Funders: National Heart, Lung, and Blood Institute, National Institute of Diabetes and Digestive and Kidney Diseases

Awards: COMPREHENSIVE SICKLE CELL CENTER, G2373958829, DEVELOPMENTAL BIOLOGY OF HUMAN ERYTHROPOIESIS

OpenAlex ID: W1966125216

FWCI: 7.802

Cites: 33

Cited by: 214

Related to: 10