Double missense mutation in exon 41 of the human dystrophin gene detected by double strand conformation analysis
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference26 articles.
1. Identification of a mutation in the promoter region of the dystrophin gene in a patient with atypical Becker muscular dystrophy
2. Duchenne muscular dystrophy and idiopathic hyperCKemia segregating in a family
3. Familial X-linked myalgia and cramps: A nonprogressive myopathy associated with a deletion in the dystrophin gene
4. Intrafamilial variability of X-linked progressive muscular dystrophy
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4. Cardiomyopathie dilatée et toxicité musculaire des hypolipémiants : une maladie de Becker de révélation tardive;La Revue de Médecine Interne;2005-12
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