Work

The Activin Receptor-Like Kinase 1 Gene: Genomic Structure and Mutations in Hereditary Hemorrhagic Telangiectasia Type 2

Year: 1997

Type: article

Study design: Observational Study

Source: The American Journal of Human Genetics

DOI: 10.1086/513903

Authors: Jonathan N. Berg, Carol J. Gallione, Timothy T. Stenzel, David W. Johnson, William P. Allen, Charles E. Schwartz, Charles E. Jackson, Mary E.M. Porteous, Douglas A. Marchuk

Institutions: Duke Medical Center, University of Edinburgh, Greenwood Genetic Center, Henry Ford Hospital

Language: English

Topic: Vascular Anomalies and Treatments

Subfield: Genetics

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: National Institutes of Health, National Heart, Lung, and Blood Institute, H2020 European Research Council

Awards: GENETICS OF HEREDITARY HEMORRHAGIC TELANGIECTASIA, DIVERSITY OF TGF BETA RECEPTOR MUTATIONS IN HHT SYNDROME, G2962129691, MOLECULAR PATHOLOGY OF HHT (OSLER/WEBER/RENDU DISEASE), G416562823, G4504593300

OpenAlex ID: W2007431373

FWCI: 5.978

Cites: 35

Cited by: 242

Related to: 10