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Genetic analysis of 1051 Chinese families with Duchenne/Becker Muscular Dystrophy.

Xiangdong KongXingjian ZhongLina LiuSiying CuiYuxia YangLingrong Kong
Published in: BMC medical genetics (2019)
Our results expand the spectrum of DMD mutations, which could contribute to the treatment of DMD/BMD and provide an effective diagnosis method. Thus, the combination of MLPA, NGS and Sanger sequencing is of great significance for family analysis, gene diagnosis and gene therapy.
Keyphrases
  • muscular dystrophy
  • gene therapy
  • duchenne muscular dystrophy
  • single cell
  • copy number
  • genome wide
  • gene expression
  • dna methylation