Fig. 3From: A case report: Becker muscular dystrophy presenting with epilepsy and dysgnosia induced by duplication mutation of Dystrophin geneMultiplex ligation-dependent probe amplification of the DNA extracted from peripheral blood showed a duplication mutation in exons 37–44 in the Dystrophin gene (fluorescence intensity 1.81–2.18; normal range 0.7–1.33)Back to article page