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Judge, Daniel P.

https://orcid.org/0000-0002-3407-0248

A5076454382 | I153297377

Mayo Clinic

Medical University of South Carolina

Citations 22

HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies

Europace | August 2, 2011 | Volume: 13 | Issue: 8 | Pages: 1077-1109

10.1093/europace/eur245 | PMID 21810866

Mutations in Fibrillin-1 Cause Congenital Scleroderma: Stiff Skin Syndrome

Science Translational Medicine | March 17, 2010 | Volume: 2 | Issue: 23 | Pages: No page available

10.1126/scitranslmed.3000488 | PMID 20375004

Stiff skin syndrome, an autosomal dominant congenital form of scleroderma, is caused by mutations in the domain of fibrillin-1 that mediates integrin binding.