Relationship between fibrillin-1 genotype and severity of cardiovascular involvement in Marfan syndrome
Author:
Publisher
BMJ
Subject
Cardiology and Cardiovascular Medicine
Reference20 articles.
1. Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene;Dietz;Nature,1991
2. The risk for type B aortic dissection in Marfan syndrome;den Hartog;J Am Coll Cardiol,2015
3. Diagnosis and genetics in Marfan syndrome. Diagnosis and genetics of Marfan syndrome;Franken;Expert Opin Orphan Drugs,2014
4. Beneficial outcome of losartan therapy depends on type of FBN1 mutation in Marfan syndrome;Franken;Circ Cardiovasc Genet,2015
5. Increased frequency of FBN1 truncating and splicing variants in Marfan syndrome patients with aortic events;Baudhuin;Genet Med,2015
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