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Mutation Spectrum of Dystrophin Gene in Malaysian Patients with Duchenne/Becker Muscular Dystrophy

✍ Scribed by Rani, Abdul Qawee; Sasongko, Teguh Haryo; Sulong, Sarina; Bunyan, David; Salmi, Abdul Razak; Zilfalil, Bin Alwi; Matsuo, Masafumi; Zabidi-Hussin, Z. A. M. H.

Book ID
119965936
Publisher
Informa plc
Year
2013
Tongue
English
Weight
132 KB
Volume
27
Category
Article
ISSN
0167-7063

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DGGE-based whole-gene mutation scanning
DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients
✍ Robert M.W. Hofstra; Inge M. Mulder; Rolf Vossen; Pia A. M. de Koning-Gans; Mari πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 224 KB

## Communicated by Ulf Landegren Duchenne and Becker muscular dystrophy (DMD and BMD) are caused by mutations in the dystrophin gene. Large rearrangements in the gene are found in about two-thirds of DMD patients, with B60% carrying deletions and 5-10% carrying duplications. Most of the remaining