Literature DB >> 6881909

Genetic linkage between the loci for myotonic dystrophy and peptidase D.

T O'Brien, S Ball, M Sarfarazi, P S Harper, E B Robson.   

Abstract

In a linkage study between myotonic dystrophy and peptidase D it is evident from the lod score values that with high probability theta lies between 0 and 0.1. The data thus support a previous hint of linkage between peptidase D and the Lutheran and secretor loci, which were already known to be linked to myotonic dystrophy.

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Year:  1983        PMID： 6881909     DOI： 10.1111/j.1469-1809.1983.tb00978.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN： 0003-4800            Impact factor:   1.670


  15 in total

1.  The human prolidase gene: structure and restriction fragment length polymorphisms.

Authors:  A Tanoue; F Endo; I Matsuda
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

Review 2.  Gene mapping and chromosome 19.

Authors:  D J Shaw; J D Brook; A L Meredith; H G Harley; M Sarfarazi; P S Harper
Journal:  J Med Genet       Date:  1986-02       Impact factor: 6.318

3.  Linkage analysis of peripheral neurofibromatosis (Von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophy.

Authors:  S M Huson; A L Meredith; M Sarfarazi; D J Shaw; D A Compston; P S Harper
Journal:  J Med Genet       Date:  1986-02       Impact factor: 6.318

4.  Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19.

Authors:  D J Shaw; A L Meredith; M Sarfarazi; H G Harley; S M Huson; J D Brook; L Bufton; M Litt; T Mohandas; P S Harper
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132

5.  Localisation of genetic markers and orientation of the linkage group on chromosome 19.

Authors:  J D Brook; D J Shaw; L Meredith; G A Bruns; P S Harper
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

6.  Molecular defect in siblings with prolidase deficiency and absence or presence of clinical symptoms. A 0.8-kb deletion with breakpoints at the short, direct repeat in the PEPD gene and synthesis of abnormal messenger RNA and inactive polypeptide.

Authors:  A Tanoue; F Endo; I Akaboshi; T Oono; J Arata; I Matsuda
Journal:  J Clin Invest       Date:  1991-04       Impact factor: 14.808

7.  Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19q.

Authors:  U Friedrich; H Brunner; D Smeets; E Lambermon; H H Ropers
Journal:  Hum Genet       Date:  1987-03       Impact factor: 4.132

8.  Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.

Authors:  K E Davies; J Jackson; R Williamson; P S Harper; S Ball; M Sarfarazi; L Meredith; G Fey
Journal:  J Med Genet       Date:  1983-08       Impact factor: 6.318

9.  Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19.

Authors:  J A Donald; S C Wallis; A Kessling; P Tippett; E B Robson; S Ball; K E Davies; P Scambler; K Berg; A Heiberg
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

10.  The locus for apolipoprotein E (apoE) is close to the Lutheran (Lu) blood group locus on chromosome 19.

Authors:  T Gedde-Dahl; B Olaisen; P Teisberg; M C Wilhelmy; B Mevåg; R Helland
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132
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