Work

BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies

Year: 2008

Type: article

Study design: Observational Study

Source: Blood Cells Molecules and Diseases

DOI: 10.1016/j.bcmd.2008.06.007

Authors: Amanda E. Sedgewick, Nadia Timofeev, Paola Sebastiani, Jason C.C. So, Edmond S.K. Ma, Li Chong Chan, Goonnapa Fucharoen, Supan Fucharoen, Cynara G. Barbosa, Badri N. Vardarajan, Lindsay A. Farrer, Clinton T. Baldwin, Martin H. Steinberg, David H.K. Chui

Institutions: Boston University, Queen Mary Hospital, University of Hong Kong, Khon Kaen University

Language: English

Topic: Hemoglobinopathies and Related Disorders

Subfield: Genetics

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: green

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

Awards: Genetic Modulation of Sickle Cell Disease, G332598346, Boston Comprehensive Sickle Cell Center, Genetic Modulation of HbF in Beta Thalassemia, G4410414779, G4475704305, G4701717143, Interdisciplinary Training for Biostatisticians

OpenAlex ID: W2049584544

FWCI: 7.763

Cites: 13

Cited by: 172

Related to: 10