Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10

[1]  Melanie E. Goward,et al.  The DNA sequence of human chromosome 22 , 1999, Nature.

[2]  Melvin G McInnis,et al.  Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12 , 1999, Nature Genetics.

[3]  T. Bird,et al.  An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8) , 1999, Nature Genetics.

[4]  H. Zoghbi,et al.  Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy , 1999, Annals of neurology.

[5]  S. Pulst,et al.  Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22. , 1999, American journal of human genetics.

[6]  M. Pericak-Vance,et al.  A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17q. , 1998, Genomics.

[7]  F. McMahon,et al.  A novel, heritable, expanding CTG repeat in an intron of the SEF2-1 gene on chromosome 18q21.1. , 1997, Human molecular genetics.

[8]  Y. Agid,et al.  Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion , 1997, Nature Genetics.

[9]  Georg Auburger,et al.  Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2 , 1996, Nature Genetics.

[10]  Yves Agid,et al.  Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats , 1996, Nature Genetics.

[11]  S. Tsuji,et al.  Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT , 1996, Nature Genetics.

[12]  Y. Agid,et al.  Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias , 1995, Nature.

[13]  Huda Y. Zoghbi,et al.  Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1 , 1993, Nature Genetics.

[14]  T. Hudson,et al.  Direct detection of novel expanded trinucleotide repeats in the human genome , 1993, Nature Genetics.

[15]  P. Patel,et al.  The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure. , 1998, American journal of human genetics.

[16]  T. Bird,et al.  Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA , 1998, Nature Genetics.

[17]  S. Warren,et al.  Genetic instabilities and hereditary neurological diseases , 1998 .

[18]  William B. Dobyns,et al.  Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel , 1997, Nature Genetics.

[19]  Shigenobu Nakamura,et al.  CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1 , 1994, Nature Genetics.