Myotonic Dystrophy Type 2: Human Founder Haplotype and Evolutionary Conservation of the Repeat Tract

This publication has 27 references indexed in Scilit:

• Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of ZNF9
  Science, 2001
• The tetranucleotide UCAY directs the specific recognition of RNA by the Nova K-homology 3 domain
  Proceedings of the National Academy of Sciences, 2000
• Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
  Nature Genetics, 1996
• Organization of the gene encoding cellular nucleic acid-binding protein
  Gene, 1995
• Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles
  Cell, 1994
• Myotonic dystrophy with no trinucleotide repeat expansion
  Annals of Neurology, 1994
• Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I
  Nature Genetics, 1993
• Mutation of human short tandem repeats
  Human Molecular Genetics, 1993
• Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member
  Published by Elsevier ,1992
• Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy
  Nature, 1992