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Molecular analysis of the duchenne muscular dystrophy gene in patients with becker muscular dystrophy presenting with dilated cardiomyopathy

โœ Scribed by Dr. Kunihiro Yoshida; Dr. Shu-Ichi Ikeda; Dr. Akinori Nakamura; Dr. Mitsuru Kagoshima; Dr. Shin'ichi Takeda; Dr. Shin'ichi Shoji; Dr. Nobuo Yanagisawa

Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
656 KB
Volume
16
Category
Article
ISSN
0148-639X

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DGGE-based whole-gene mutation scanning
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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