Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Yuan-Ren Tong"'
Autor:
Yuan-Ren Tong, Chang Geng, Yu-Zhou Guan, Yan-Huan Zhao, Hai-Tao Ren, Feng-Xia Yao, Chao Ling, Dan-Chen Wang, Lin Chen, Li-Ying Cui, Shu-Yang Zhang, Yi Dai
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are X-linked recessive neuromuscular disorders caused by mutations in DMD. A high-quality database of DMD/BMD is essential not only for clinical practice but also for fundamental r
Externí odkaz:
https://doaj.org/article/b39a3e834c0b4f7e9ef083687870c441
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 12 (2021)
Frontiers in Genetics, Vol 12 (2021)
Purpose: Exon deletions make up to 80% of mutations in the DMD gene, which cause Duchenne and Becker muscular dystrophy. Exon 45-55 regions were reported as deletion hotspots and intron 44 harbored more than 25% of deletion start points. We aimed to
Autor:
Chang Geng, Yi Dai, Chao Ling, Dan-Chen Wang, Haitao Ren, Fengxia Yao, Yuan-Ren Tong, Shuyang Zhang, Liying Cui, Lin Chen, Yuzhou Guan, Yanhuan Zhao
Publikováno v:
Frontiers in Neurology
Frontiers in Neurology, Vol 11 (2020)
Frontiers in Neurology, Vol 11 (2020)
Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are X-linked recessive neuromuscular disorders caused by mutations in DMD. A high-quality database of DMD/BMD is essential not only for clinical practice but also for fundamental r