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  • Eloisa Arbustini, Maurizia Grasso, +19 authors Luigi Tavazzi
  • Biology, Medicine
  • Human mutation
  • 2005 (First Publication: 1 November 2005)
  • Marfan Syndrome (MFS) is an autosomal dominant disorder of the connective tissue due to mutations of Fibrillin-1 gene (FBN1) in more than 90% of cases and Transforming Growth Factor-Beta-Receptor2Expand