Title Molecular Characterization Of Dystrophin Gene In A Sample Of Iraqi Patients With Muscular Dystrophy Year 2013

@inproceedings{Tahrir2014TitleMC,
  title={Title Molecular Characterization Of Dystrophin Gene In A Sample Of Iraqi Patients With Muscular Dystrophy Year 2013},
  author={Areen Tahrir and Ramadhan Al-Hadithi},
  year={2014}
}
  • Areen Tahrir, Ramadhan Al-Hadithi
  • Published 2014
Background: Dystrophinopathies are the commonest forms of muscular dystrophy and comprise clinically recognized forms, Duchenne Muscular Dystrophy (DMD), and Becker Muscular Dystrophy (BMD). Mutations in the dystrophin gene which consist of large gene deletions (65%), duplications (5%) and point mutations (30%) are responsible for reducing the amount of… CONTINUE READING