Literature DB >> 7438789

Linkage studies on glyoxalase I (GLO), pepsinogen (PG), spinocerebellar ataxia (SCA1), and HLA.

J E Whittington, B J Keats, J F Jackson, R D Currier, P I Terasaki.   

Abstract

Pedigree analyses of five families in which a form of spinocerebellar ataxia (SCA1) is present have been used to obtain additional information on the location of SCA1 on chromosome 6. Recombination rates with HLA and glyoxalase I (GLO) suggest that the order is HLA-GLO-SCA1. There was no evidence for linkage of pepsinogen isozyme-5 (PG) either to HLA or GLO.

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Year:  1980        PMID： 7438789     DOI： 10.1159/000131524

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


  4 in total

1.  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

2.  The gene encoding vasoactive intestinal peptide is located on human chromosome 6p21----6qter.

Authors:  I Gozes; R Avidor; Y Yahav; D Katznelson; C M Croce; K Huebner
Journal:  Hum Genet       Date:  1987-01       Impact factor: 4.132

3.  Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p.

Authors:  L P Ranum; L A Duvick; S S Rich; L J Schut; M Litt; H T Orr
Journal:  Am J Hum Genet       Date:  1991-07       Impact factor: 11.025

4.  Spinocerebellar ataxia: localization of an autosomal dominant locus between two markers on human chromosome 6.

Authors:  S S Rich; P Wilkie; L Schut; G Vance; H T Orr
Journal:  Am J Hum Genet       Date:  1987-10       Impact factor: 11.025
  4 in total

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