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MLPA analysis/complete sequencing of the DMD gene in a group of Bulgarian Duchenne/Becker muscular dystrophy patients

โœ Scribed by Albena Todorova; Tihomir Todorov; Bilyana Georgieva; Michaela Lukova; Velina Guergueltcheva; Ivo Kremensky; Vanyo Mitev

Book ID
116793775
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
212 KB
Volume
18
Category
Article
ISSN
0960-8966

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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
โœ Robert M.W. Hofstra; Inge M. Mulder; Rolf Vossen; Pia A. M. de Koning-Gans; Mari ๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 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