𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome

✍ Scribed by Chia-Cheng Hung; Shin-Yu Lin; Chien-Nan Lee; Hui-Yu Cheng; Shuan-Pei Lin; Ming-Ren Chen; Chih-Ping Chen; Chien-Hui Chang; Chiou-Ya Lin; Chih-Chieh Yu; Hsin-Hui Chiu; Wen-Fang Cheng; Hong-Nerng Ho; Dau-Ming Niu; Yi-Ning Su


Book ID
111111522
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
119 KB
Volume
73
Category
Article
ISSN
0003-4800

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Identification of 29 novel and nine recu
✍ Kathrin Rommel; Matthias Karck; Axel Haverich; Yskert von Kodolitsch; Meike Rybc πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 180 KB

## Communicated by Jurgen Horst Marfan syndrome (MFS) is an autosomal-dominant disorder of the fibrous connective tissue that is typically caused by mutations in the gene coding for fibrillin-1 (FBN1), a major component of extracellular microfibrils. The clinical spectrum of MFS is highly variable