Work

Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders

Year: 1995

Type: article

Source: Human Molecular Genetics

DOI: 10.1093/hmg/4.suppl_1.1799

Authors: HC Dietz, RE Pyeritz

Institutions: Johns Hopkins University, Johns Hopkins Medicine

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 Heart, Lung, and Blood Institute, National Center for Research Resources

Awards: GENERAL CLINICAL RESEARCH CENTER, DEVELOPMENT OF A TRANSGENIC MODEL OF THE MARFAN SYNDROME, CONGENITAL HEART DISEASE--MODELING AND GENETIC ANALYSIS

OpenAlex ID: W2170121771

FWCI: 12.19

Cites:

Cited by: 485

Related to: 10