Literature DB >> 3397063

Two different genes for X-linked retinitis pigmentosa.

B Wirth1, M J Denton, J D Chen, M Neugebauer, F B Halliday, M van Schooneveld, J Donald, E M Bleeker-Wagemakers, P L Pearson, A Gal.   

Abstract

Linkage analysis was carried out in three large multigenerational kindreds with X-linked retinitis pigmentosa using DNA markers on Xp. About 10% recombination has been found between the retinitis pigmentosa locus (RP2) and the marker locus DXS7, assigned to band Xp11.3, which was reported earlier to be closely linked to RP2 in several independent families. In the kindreds described in this paper, however, RP2 shows close linkage and no recombination with the marker loci OTC and DXS148, both assigned to Xp21, indicating that, contrary to previous linkage studies, there is evidence of an RP locus distal to DXS7. This suggests that X-linked retinitis pigmentosa is genetically heterogeneous, i.e., caused by mutations at different loci.

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Year:  1988        PMID: 3397063     DOI: 10.1016/0888-7543(88)90011-0

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  10 in total

1.  Clinical and genetic heterogeneity in retinitis pigmentosa.

Authors:  J Kaplan; D Bonneau; J Frézal; A Munnich; J L Dufier
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

2.  Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred.

Authors:  A F Wright; S S Bhattacharya; M A Aldred; M Jay; A D Carothers; N S Thomas; A C Bird; B Jay; H J Evans
Journal:  J Med Genet       Date:  1991-07       Impact factor: 6.318

3.  Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pigmentosa families.

Authors:  M A Musarella; L Anson-Cartwright; S M Leal; L D Gilbert; R G Worton; G A Fishman; J Ott
Journal:  Genomics       Date:  1990-10       Impact factor: 5.736

4.  Linkage heterogeneity between X-linked retinitis pigmentosa and a map of 10 RFLP loci.

Authors:  J D Chen; F Halliday; G Keith; L Sheffield; P Dickinson; R Gray; I Constable; M Denton
Journal:  Am J Hum Genet       Date:  1989-09       Impact factor: 11.025

5.  Linkage of X-linked retinitis pigmentosa to the hypervariable DNA marker M27 beta (DXS255).

Authors:  T Meitinger; N A Fraser; B Lorenz; E Zrenner; J Murken; I W Craig
Journal:  Hum Genet       Date:  1989-02       Impact factor: 4.132

6.  Phenotype-genotype correlations in X linked retinitis pigmentosa.

Authors:  J Kaplan; A Pelet; C Martin; O Delrieu; S Aymé; D Bonneau; M L Briard; A Hanauer; L Larget-Piet; P Lefrançois
Journal:  J Med Genet       Date:  1992-09       Impact factor: 6.318

7.  Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).

Authors:  H K Hong; R E Ferrell; M B Gorin
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

8.  Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests.

Authors:  J Ott; S Bhattacharya; J D Chen; M J Denton; J Donald; C Dubay; G J Farrar; G A Fishman; D Frey; A Gal
Journal:  Proc Natl Acad Sci U S A       Date:  1990-01       Impact factor: 11.205

9.  Synaptophysin: structure of the human gene and assignment to the X chromosome in man and mouse.

Authors:  T Ozçelik; R G Lafreniere; B T Archer; P A Johnston; H F Willard; U Francke; T C Südhof
Journal:  Am J Hum Genet       Date:  1990-09       Impact factor: 11.025

10.  Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia.

Authors:  F P Cremers; D J van de Pol; B Wieringa; F S Collins; E M Sankila; V M Siu; W F Flintoff; F Brunsmann; L A Blonden; H H Ropers
Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

  10 in total

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