Work

Novel Fibrillin 1 Mutation in a Case of Neonatal Marfan Syndrome: The Increasing Importance of Early Recognition

Year: 2007

Type: article

Study design: Case Report

Source: Congenital Heart Disease

DOI: 10.1111/j.1747-0803.2007.00123.x

Authors: Jamie Sutherell, Yuri Zarate, Bradley T. Tinkle, Larry W. Markham, Linda H. Cripe, James C. Hyland, David Witte, Robert J. Hopkin, Robert B. Hinton

Institution: Cincinnati Children's Hospital Medical Center

Language: English

Topic: Connective tissue disorders research

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

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

Awards: G1541964068, Genetic and Developmental Basis of Pediatric Aortic Valve Disease Pathogenesis

OpenAlex ID: W2158303630

FWCI:

Cites: 17

Cited by: 20

Related to: 10