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Disease Markers
Volume 25, Issue 2, Pages 115-121

Sensitivity and Frequencies of Dystrophin Gene Mutations in Thai DMD/BMD Patients As Detected by Multiplex PCR

Thanyachai Sura, Jakris Eu-ahsunthornwattana, Sarinee Pingsuthiwong, and Manisa Busabaratana

Division of Medical Genetics & Molecular Medicine and Academic Center for Medical Genetics, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand

Received 8 October 2008; Accepted 8 October 2008

Copyright © 2008 Hindawi Publishing Corporation. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Citations to this Article [5 citations]

The following is the list of published articles that have cited the current article.

  • Qian Wang, Xiaofeng Yang, Yang Yan, Nan Song, Changkun Lin, and Chunlian Jin, “Duchenne or Becker muscular dystrophy: A clinical, genetic and immunohistochemical study in China,” Neurology India, vol. 59, no. 6, pp. 797–802, 2011. View at Publisher · View at Google Scholar
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  • Yuanyuan Li, Zhuo Liu, Shengrong OuYang, Yanli Zhu, Liwen Wang, and Jianxin Wu, “Distribution of dystrophin gene deletions in a Chinese population,” Journal Of International Medical Research, vol. 44, no. 1, pp. 99–108, 2016. View at Publisher · View at Google Scholar
  • Sara C. Atehortúa, Luz H. Lugo, Mateo Ceballos, Esteban Orozco, Paula A. Castro, Juan C. Arango, and Heidi E. Mateus, “Cost-Effectiveness Analysis of Diagnosis of Duchenne/Becker Muscular Dystrophy in Colombia,” Value in Health Regional Issues, vol. 17, pp. 1–6, 2018. View at Publisher · View at Google Scholar