Marfan Syndrome (MfS) is an autosomal dominant inherited connective tissue disorder with variable phenotypic expression of cardiovascular, skeletal and ocular manifestations. Cardiovascular complications, such as aortic aneurysm and dissection drastically reduce life expectancy of individuals with M
β¦ LIBER β¦
A novelde novomutation in exon 14 of the fibrillin-1 gene associated with delayed secretion of fibrillin in a patient with a mild Marfan phenotype
β Scribed by Patrick Booms; Anne P. Withers; Maureen Boxer; Ursula C. Kaufmann; Christian Hagemeier; Ulrich Vetter; P. N. Robinson
- Book ID
- 106136703
- Publisher
- Springer
- Year
- 1997
- Tongue
- English
- Weight
- 71 KB
- Volume
- 100
- Category
- Article
- ISSN
- 0340-6717
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