Literature DB >> 8133496

Mutation size and age at onset in Huntington's disease.

D Craufurd1, A Dodge.   

Abstract

The mutation responsible for Huntington's disease is a polymorphic (CAG)n repeat sequence which is expanded on affected chromosomes. The number of repeat units observed on 229 affected chromosomes varied from 27 to 102, while the control chromosomes showed a range of 7 to 34 repeats. There was a highly significant relationship between the size of the expanded region and age at onset, larger mutations being associated with earlier onset. This association was strongest in those with onset before 25 years of age but less clear cut with later onset, and is therefore unlikely to be useful for predicting age at onset in the context of presymptomatic testing.

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Year:  1993        PMID: 8133496      PMCID: PMC1016633          DOI: 10.1136/jmg.30.12.1008

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  3 in total

1.  Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.

Authors:  A J Verkerk; M Pieretti; J S Sutcliffe; Y H Fu; D P Kuhl; A Pizzuti; O Reiner; S Richards; M F Victoria; F P Zhang
Journal:  Cell       Date:  1991-05-31       Impact factor: 41.582

2.  The natural history of Huntington disease: possible role of "aging genes".

Authors:  L A Farrer; P M Conneally; P L Yu
Journal:  Am J Med Genet       Date:  1984-05

3.  Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

Authors:  J D Brook; M E McCurrach; H G Harley; A J Buckler; D Church; H Aburatani; K Hunter; V P Stanton; J P Thirion; T Hudson
Journal:  Cell       Date:  1992-02-21       Impact factor: 41.582

  3 in total
  9 in total

Review 1.  Huntington disease--another chapter rewritten.

Authors:  M A Nance
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

Review 2.  The genetic defect causing Huntington's disease: repeated in other contexts?

Authors:  J F Gusella; F Persichetti; M E MacDonald
Journal:  Mol Med       Date:  1997-04       Impact factor: 6.354

3.  Trinucleotide repeat length and progression of illness in Huntington's disease.

Authors:  K Kieburtz; M MacDonald; C Shih; A Feigin; K Steinberg; K Bordwell; C Zimmerman; J Srinidhi; J Sotack; J Gusella
Journal:  J Med Genet       Date:  1994-11       Impact factor: 6.318

Review 4.  A specific mutation for Huntington's disease.

Authors:  P S Harper
Journal:  J Med Genet       Date:  1993-12       Impact factor: 6.318

5.  The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size.

Authors:  R R Brinkman; M M Mezei; J Theilmann; E Almqvist; M R Hayden
Journal:  Am J Hum Genet       Date:  1997-05       Impact factor: 11.025

6.  Lentiviral-mediated delivery of mutant huntingtin in the striatum of rats induces a selective neuropathology modulated by polyglutamine repeat size, huntingtin expression levels, and protein length.

Authors:  Luis Pereira de Almeida; Christopher A Ross; Diana Zala; Patrick Aebischer; Nicole Déglon
Journal:  J Neurosci       Date:  2002-05-01       Impact factor: 6.167

7.  Ideomotor limb apraxia in Huntington's disease: a case-control study.

Authors:  Anna K Hödl; Elfriede Hödl; Daniela V Otti; Brigitte Herranhof; Rottraut Ille; Raphael M Bonelli
Journal:  J Neurol       Date:  2008-03-04       Impact factor: 4.849

8.  Large-scale phenome analysis defines a behavioral signature for Huntington's disease genotype in mice.

Authors:  Vadim Alexandrov; Dani Brunner; Liliana B Menalled; Andrea Kudwa; Judy Watson-Johnson; Matthew Mazzella; Ian Russell; Melinda C Ruiz; Justin Torello; Emily Sabath; Ana Sanchez; Miguel Gomez; Igor Filipov; Kimberly Cox; Mei Kwan; Afshin Ghavami; Sylvie Ramboz; Brenda Lager; Vanessa C Wheeler; Jeff Aaronson; Jim Rosinski; James F Gusella; Marcy E MacDonald; David Howland; Seung Kwak
Journal:  Nat Biotechnol       Date:  2016-07-04       Impact factor: 54.908

9.  Pathological cell-cell interactions are necessary for striatal pathogenesis in a conditional mouse model of Huntington's disease.

Authors:  Xiaofeng Gu; Véronique M André; Carlos Cepeda; Shi-Hua Li; Xiao-Jiang Li; Michael S Levine; X William Yang
Journal:  Mol Neurodegener       Date:  2007-04-30       Impact factor: 14.195

  9 in total

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