High levels of somatic DNA diversity at the myotonic dystrophy type 1 locus are driven by ultra-frequent expansion and contraction mutations

समान संसाधन

• Somatic instability of the expanded CTG triplet repeat in myotonic dystrophy type 1 is a heritable quantitative trait and modifier of disease severity
  द्वारा: Higham, Catherine
  प्रकाशित: (2012)
• Molecular characterization of a region of DNA associated with mutations at the agouti locus in the mouse
  द्वारा: Bultman, S. J.
  प्रकाशित: (1991)
• High mitochondrial mutation rates estimated from deep-rooting Costa Rican pedigrees
  द्वारा: Castri, Loredana
  प्रकाशित: (2012)
• Analysis of mutational dynamics at the DMPK (CTG)n locus identifies saliva as a suitable DNA sample source for genetic analysis in myotonic dystrophy type 1
  द्वारा: Corrales Acuña, Eyleen Vanessa
  प्रकाशित: (2019)
• Phenylketonuria in Costa Rica: preliminary spectrum of PAH mutations and their associations with highly polymorphic haplotypes
  द्वारा: Santos Pasamontes, María
  प्रकाशित: (1996)