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Single-molecule optical mapping enables quantitative measurement of D4Z4 repeats in facioscapulohumeral muscular dystrophy (FSHD).

Yi DaiPidong LiZhiqiang WangFan LiangFan YangLi FangYu HuangShangzhi HuangJiapeng ZhouDepeng WangLiying CuiKai Wang
Published in: Journal of medical genetics (2019)
While the study is limited by small sample size, our results demonstrated that single-molecule optical mapping is a viable approach for more refined analysis on genotype-phenotype relationships in FSHD, especially when postzygotic mosaicism is present.
Keyphrases
  • single molecule
  • muscular dystrophy
  • high resolution
  • atomic force microscopy
  • living cells
  • duchenne muscular dystrophy
  • high speed
  • mass spectrometry
  • high density