Marfan syndrome (MFS) is an autosomal dominant connective tissue disorder characterized by manifestations in the cardiovascular, skeletal, ocular, and other organ systems. MFS type1 (MFS1) is caused by mutations in the gene encoding fibrillin (FBN1). Recently, the transforming growth factor-beta rec
β¦ LIBER β¦
Duplication of the TGFBR1 gene causes features of Loeys-Dietz syndrome
β Scribed by Jeroen Breckpot; Werner Budts; Francis De Zegher; Joris R. Vermeesch; Koenraad Devriendt
- Book ID
- 116433300
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 378 KB
- Volume
- 53
- Category
- Article
- ISSN
- 1769-7212
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