Work

Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly

Year: 2008

Type: article

Study design: Observational Study

Source: The American Journal of Human Genetics

DOI: 10.1016/j.ajhg.2008.05.012

Authors: Erich Roessler, Maia V. Ouspenskaia, Jayaprakash D. Karkera, Jorge I. Vélez, Amy Kantipong, Felicitas Lacbawan, Peter Bowers, John W. Belmont, Jeffrey A. Towbin, Elizabeth Goldmuntz, Benjamin Feldman, Maximilian Muenke

Institutions: National Institutes of Health, National Human Genome Research Institute, Yale University, Baylor College of Medicine, Children's Hospital of Philadelphia

Language: English

Topic: Congenital heart defects research

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: National Institutes of Health, National Heart, Lung, and Blood Institute, National Human Genome Research Institute

Awards: G2198599887, Novel Genomic Disorders Causing Cardiovascular Malformations, Genetic Mechanisms in Pediatric Heart Disease, G55554327

OpenAlex ID: W2072151865

FWCI: 6.589

Cites: 38

Cited by: 178

Related to: 10