Somatic instability of the expanded CTG triplet repeat in myotonic dystrophy type 1 is a heritable quantitative trait and modifier of disease severity

Ítems similars

• Longitudinal increases in somatic mosaicism of the expanded CTG repeat in myotonic dystrophy type 1 are associated with variation in age-at-onset
  per: Morales Montero, Fernando
  Publicat: (2020)
• High levels of somatic DNA diversity at the myotonic dystrophy type 1 locus are driven by ultra-frequent expansion and contraction mutations
  per: Higham, Catherine
  Publicat: (2012)
• A polymorphism in the MSH3 mismatch repair gene is associated with the levels of somatic instability of the expanded CTG repeat in the blood DNA of myotonic dystrophy type 1 patients
  per: Morales Montero, Fernando
  Publicat: (2016)
• Individual-specific levels of CTG•CAG somatic instability are shared across multiple tissues in myotonic dystrophy type 1
  per: Morales Montero, Fernando
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• MSH3 modifies somatic instability and disease severity in Huntington’s and myotonic dystrophy type 1
  per: Flower, Michael
  Publicat: (2019)