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Publication details
Point mutations in Czech DMD/BMD patients and their phenotypic outcome
Authors | |
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Year of publication | 2009 |
Type | Article in Periodical |
Magazine / Source | Neuromuscular Disorders |
MU Faculty or unit | |
Citation | |
Field | Genetics and molecular biology |
Keywords | Duchene muscular dystrophy; DMD; BMD |
Description | Duchenne and Becker muscular dystrophies (DMD/BMD) are associated with mutations in the DMD gene. We determined the mutation status of 47 patients with dystrophinopathy without deletion or duplication in the DMD gene. Further, using quantitative analysis of DMD mRNA carrying various mutated alleles, we examine levels of mRNA degradation due to nonsense mediated mRNA decay. The quantity of dystrophin mRNA is different depending on the presence of a mutation leading to a premature termination codon, and position of the analysed mRNA region with respect to its 5 end or 3 end. |
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