Abstract
Marfan syndrome is an autosomal, dominant, heritable disorder of connective tissue characterized by defects in the skeletal, ocular, and cardiovascular systems. Marfan syndrome is caused by mutations in the gene encoding fibrillin-1 ....
| Original language | English (US) |
|---|---|
| Title of host publication | xPharm |
| Subtitle of host publication | The Comprehensive Pharmacology Reference |
| Publisher | Elsevier Inc. |
| Pages | 1-6 |
| Number of pages | 6 |
| ISBN (Print) | 9780080552323 |
| DOIs | |
| State | Published - 2007 |
ASJC Scopus subject areas
- Pharmacology, Toxicology and Pharmaceutics(all)