Literature DB >> 857157

Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing.

J F Jackson, R D Currier, P I Terasaki, N E Morton.   

Abstract

To determine the possibility of genetic linkage of spinocerebellar ataxia with the histocompatibility loci, we performed HLA typing and linkage analysis on 19 members of a kindred in which spinocerebellar ataxia was segregating in an autosomal dominant inheritance pattern. The ataxia locus was located on chromosome 6 at 12-cM distance from the HLA complex with lod score of 3.15 (odds is greater than 1400:1 favoring linkage over chance findings). Thus, the presence of the ataxia gene in members of this kindred at risk can be predicted with about 90 per cent accuracy by means of HLA typing in informative matings.

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Year:  1977        PMID: 857157     DOI: 10.1056/NEJM197705192962003

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


  33 in total

1.  Clinical and genetic study of a family with spinocerebellar ataxia type 1 (SCA1) and beta-thalassemia.

Authors:  V Pietrini; M Godani; S Calzetti; A Negrotti; B Castellotti; M C Riggio; C Toffoli
Journal:  Ital J Neurol Sci       Date:  1998-12

Review 2.  Neurogenetics: single gene disorders.

Authors:  S-M Pulst
Journal:  J Neurol Neurosurg Psychiatry       Date:  2003-12       Impact factor: 10.154

Review 3.  SCA1-phosphorylation, a regulator of Ataxin-1 function and pathogenesis.

Authors:  Harry T Orr
Journal:  Prog Neurobiol       Date:  2012-04-16       Impact factor: 11.685

4.  Spinocerebellar ataxia: multipoint linkage analysis of genes associated with the disease locus.

Authors:  P J Wilkie; L J Schut; S S Rich
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

Review 5.  The inherited ataxias and the new genetics.

Authors:  S R Hammans
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-10       Impact factor: 10.154

6.  Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onset.

Authors:  L P Ranum; M Y Chung; S Banfi; A Bryer; L J Schut; R Ramesar; L A Duvick; A McCall; S H Subramony; L Goldfarb
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025

7.  The spinocerebellar ataxia 2 locus is located within a 3-cM interval on chromosome 12q23-24.1.

Authors:  R Allotey; R Twells; C Cemal; B S Norte; J Weissenbach; M Pook; R Williamson; S Chamberlain
Journal:  Am J Hum Genet       Date:  1995-07       Impact factor: 11.025

8.  The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus.

Authors:  T J Kwiatkowski; H T Orr; S Banfi; A E McCall; C Jodice; F Persichetti; A Novelletto; F LeBorgne-DeMarquoy; L A Duvick; M Frontali
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

9.  Tight linkage of the gene for spinocerebellar ataxia to D6S89 on the short arm of chromosome 6 in a kindred for which close linkage to both HLA and F13A1 is excluded.

Authors:  B J Keats; M S Pollack; A McCall; M A Wilensky; L J Ward; M Lu; H Y Zoghbi
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

10.  Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region.

Authors:  I Lopes-Cendes; E Andermann; E Attig; F Cendes; S Bosch; M Wagner; F Gerstenbrand; F Andermann; G A Rouleau
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

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