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FBN1: The disease-causing gene for Marfan syndrome and other genetic disorders
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Year:
2016
Type:
review
Source:
Gene
DOI:
10.1016/j.gene.2016.07.033
Authors:
Lynn Y. Sakai,
Douglas R. Keene,
Marjolijn Renard,
Julie De Backer
Institutions:
Oregon Health & Science University,
Shriners Hospitals for Children - Portland,
Ghent University Hospital
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:
green
Funders:
Shriners Hospitals for Children,
Vlaamse regering,
National Institutes of Health,
National Heart, Lung, and Blood Institute,
National Institute of General Medical Sciences,
National Institute of Arthritis and Musculoskeletal and Skin Diseases
show all 6
Awards:
Microfibril Fragments: Biomarkers of Aortic Disease,
Consortium for Translational Research in Marfan Syndrome,
Gene Wiki: A community-maintained knowledge base of biomedical information,
A Community Effort to Translate Protein Data to Knowledge: An Integrated Platform
OpenAlex ID:
W2480283471
FWCI:
2.134
Cites:
128
Cited by:
366
Related to:
10