Literature DB >> 2895895

A highly polymorphic locus very tightly linked to the Huntington's disease gene.

J J Wasmuth1, J Hewitt, B Smith, D Allard, J L Haines, D Skarecky, E Partlow, M R Hayden.   

Abstract

The genetic defect in Huntington's disease (HD), an inherited neuropsychiatric disorder of unknown etiology, has not been defined. The discovery of linkage between HD and the DNA marker D4S10(G8) raised the possibility of isolating the disease gene on the basis of its chromosomal location, in addition to providing a limited presymptomatic test for the late onset disorder. But it has been difficult to isolate other DNA markers nearer to the HD gene, and this has hampered attempts to identify the disease locus and limited the applicability and accuracy of predictive testing. Recently, several new DNA markers from the region of the genome near the HD gene have been isolated using a directed cloning strategy. We describe here the characterization of one of these new markers, D4S95, a highly polymorphic locus which displays no recombination with the HD gene in the families tested. The high degree of polymorphism at this locus and its proximity to the HD gene make it extremely useful for predictive testing and as a new starting point for attempts to clone the disease gene.

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Year:  1988        PMID: 2895895     DOI: 10.1038/332734a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  52 in total

1.  Predictive testing for Huntington's disease.

Authors:  P S Harper; M J Morris
Journal:  BMJ       Date:  1989-02-18

2.  Methylation at the D4S95 locus and predictive testing.

Authors:  J L Theilmann; C A Robbins; M R Hayden
Journal:  Am J Hum Genet       Date:  1989-09       Impact factor: 11.025

3.  Covariate-dependent age-at-onset distributions for Huntington disease.

Authors:  M Krawczak; B Bockel; L Sandkuijl; U Thies; I Fenton; P S Harper
Journal:  Am J Hum Genet       Date:  1991-10       Impact factor: 11.025

4.  Studies on DNA markers (D4S10 and D4S43/S127) genetically linked to Huntington's disease in Japanese families.

Authors:  I Kanazawa; I Kondo; J E Ikeda; T Ikeda; Y Shizu; M Yoshida; H Narabayashi; S Kuroda; H Tsunoda; E Mizuta
Journal:  Hum Genet       Date:  1990-08       Impact factor: 4.132

5.  The role of genetic factors in the etiology of the affective disorders.

Authors:  S Hodgkinson; M J Mullan; H M Gurling
Journal:  Behav Genet       Date:  1990-03       Impact factor: 2.805

6.  Chromosome jumping from D4S10 (G8) toward the Huntington disease gene.

Authors:  J E Richards; T C Gilliam; J L Cole; M L Drumm; J J Wasmuth; J F Gusella; F S Collins
Journal:  Proc Natl Acad Sci U S A       Date:  1988-09       Impact factor: 11.205

7.  The potential for misusing "genetic predisposition" in Canadian courts and tribunals.

Authors:  Roxanne Mykitiuk; Mark Pioro; Lilith Finkler; Jeff Nisker
Journal:  CMAJ       Date:  2011-05-24       Impact factor: 8.262

8.  Epidemiological and linkage studies on Huntington's disease in Italy.

Authors:  M Frontali; P Malaspina; C Rossi; A G Jacopini; G Vivona; M S Pergola; A Palena; A Novelletto
Journal:  Hum Genet       Date:  1990-07       Impact factor: 4.132

9.  The Huntington disease locus is most likely within 325 kilobases of the chromosome 4p telomere.

Authors:  N A Doggett; J F Cheng; C L Smith; C R Cantor
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

10.  Recombination of 4p16 DNA markers in an unusual family with Huntington disease.

Authors:  C Pritchard; N Zhu; J Zuo; L Bull; M A Pericak-Vance; J M Vance; A D Roses; A Milatovich; U Francke; D R Cox
Journal:  Am J Hum Genet       Date:  1992-06       Impact factor: 11.025

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