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

Author:

Cho Anna12,Seong Moon-Woo3,Lim Byung Chan1,Lee Hwa Jeen3,Byeon Jung Hye14,Kim Seung Soo15,Kim Soo Yeon1,Choi Sun Ah1,Wong Ai-lynn1,Lee Jeongho16,Kim Jon Soo17,Ryu Hye Won1,Lee Jin Sook18,Kim Hunmin19,Hwang Hee19,Choi Ji Eun110,Kim Ki Joong1,Hwang Young Seung1,Hong Ki Ho11,Park Seungman12,Cho Sung Im3,Lee Seung Jun3,Park Hyunwoong13,Seo Soo Hyun3,Park Sung Sup3,Chae Jong Hee1

Affiliation:

1. Department of Pediatrics; Seoul National University Children's Hospital, Seoul National University College of Medicine; Seoul Korea

2. Department of Pediatrics; Ewha Womans University School of Medicine; Seoul Korea

3. Department of Laboratory Medicine; Seoul National University College of Medicine; 101 Daehak-ro Jongno-gu Seoul 110-744 Korea

4. Department of Pediatrics; Korea University College of Medicine; Seoul Korea

5. Department of Pediatrics; Soonchunhyang University Cheonan Hospital; Chungcheongnam-do Korea

6. Department of Pediatrics; Soonchunhyang University Seoul Hospital; Seoul Korea

7. Department of Pediatrics; Daejeon Eulji University Hospital; Daejeon Korea

8. Department of Pediatrics; Gachon University Gil Medical Center; Incheon Korea

9. Department of Pediatrics; Seoul National University Bundang Hospital; Gyeonggi-do Korea

10. Department of Pediatrics; Seoul National University Boramae Medical Center; Seoul Korea

11. Department of Laboratory Medicine; Seoul Medical Center; Seoul Korea

12. Green Cross Laboratories; Yongin Korea

13. Department of Laboratory Medicine; Gyeongsang National University Hospital; Gyeongsangnam-do Korea

Funder

Korean Health Technology R&D Project, Ministry of Health & Welfare, Republic of Korea

Ewha Womans University Research Grant of 2014

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

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