Consecutive analysis of mutation spectrum in the dystrophin gene of 507 Korean boys with Duchenne/Becker muscular dystrophy in a single center

@article{Cho2017ConsecutiveAO,
  title={Consecutive analysis of mutation spectrum in the dystrophin gene of 507 Korean boys with Duchenne/Becker muscular dystrophy in a single center},
  author={A. Cho and M. Seong and B. Lim and H. J. Lee and J. Byeon and Seung Soo Kim and Soo Yeon Kim and S. Choi and Ai-Lynn Wong and Jeongho Lee and Jon Soo Kim and H. Ryu and Jin Sook Lee and Hunmin Kim and H. Hwang and Ji Eun Choi and Ki Joong Kim and Y. Hwang and Ki Ho Hong and Seungman Park and S. I. Cho and Seung Jun Lee and Hyunwoong Park and S. Seo and S. S. Park and J. Chae},
  journal={Muscle \& Nerve},
  year={2017},
  volume={55}
}
Duchenne and Becker muscular dystrophies (DMD and BMD) are allelic X‐linked recessive muscle diseases caused by mutations in the large and complex dystrophin gene. 
Mutational spectrum of dystrophinopathies in Singapore: Insights for genetic diagnosis and precision therapy
  • S. Tomar, V. Moorthy, +4 authors P. Lai
  • Medicine
  • American journal of medical genetics. Part C, Seminars in medical genetics
  • 2019
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