Literature DB >> 1979051

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

M A Musarella1, L Anson-Cartwright, S M Leal, L D Gilbert, R G Worton, G A Fishman, J Ott.   

Abstract

Using multipoint linkage analysis in 20 families segregating for X-linked retinitis pigmentosa (XLRP), the lod scores on a map of eight RFLP loci were obtained. Our results indicate that under the hypothesis of homogeneity the maximal multipoint lod score supports one disease locus located slightly distal to OTC at Xp21.1. Heterogeneity testing for two XLRP loci suggested that a second XLRP locus may be located 8.5 cM proximal to DXS28 at Xp21.3. Further heterogeneity testing for three disease loci failed to detect a third XLRP locus proximal to DXS7 in any of our 20 XLRP families.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 1979051      PMCID: PMC6174538          DOI: 10.1016/0888-7543(90)90284-2

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


  18 in total

1.  Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis.

Authors:  M A Musarella; A Burghes; L Anson-Cartwright; M M Mahtani; R Argonza; L C Tsui; R Worton
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

2.  Linkage analysis of a large Latin-American family with X-linked retinitis pigmentosa and metallic sheen in the heterozygote carrier.

Authors:  M A Musarella; L Anson-Cartwright; A Burghes; R G Worton; J G Lesko; R L Nussbaum
Journal:  Genomics       Date:  1989-05       Impact factor: 5.736

3.  X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosome.

Authors:  U Friedrich; M Warburg; P Wieacker; T F Wienker; A Gal; H H Ropers
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

4.  Mapping X-linked ophthalmic diseases: II. Linkage relationship of X-linked retinitis pigmentosa to X chromosomal short arm markers.

Authors:  R L Nussbaum; R A Lewis; J G Lesko; R Ferrell
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

5.  A primary genetic map of the pericentromeric region of the human X chromosome.

Authors:  M M Mahtani; H F Willard
Journal:  Genomics       Date:  1988-05       Impact factor: 5.736

6.  The genetic linkage map of the human X chromosome.

Authors:  D Drayna; R White
Journal:  Science       Date:  1985-11-15       Impact factor: 47.728

7.  Linkage between the X-linked retinitis pigmentosa locus and the L1.28 locus.

Authors:  S Mukai; T P Dryja; G A Bruns; J F Aldridge; E L Berson
Journal:  Am J Ophthalmol       Date:  1985-08-15       Impact factor: 5.258

8.  Xp21 DNA microdeletion in a patient with chronic granulomatous disease, retinitis pigmentosa, and McLeod phenotype.

Authors:  G de Saint-Basile; M C Bohler; A Fischer; J Cartron; J L Dufier; C Griscelli; S H Orkin
Journal:  Hum Genet       Date:  1988-09       Impact factor: 4.132

9.  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

10.  X-linked recessive retinitis pigmentosa. Clinical characteristics of carriers.

Authors:  G A Fishman; A B Weinberg; T T McMahon
Journal:  Arch Ophthalmol       Date:  1986-09
View more
  23 in total

1.  Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase.

Authors:  J B Bateman
Journal:  Trans Am Ophthalmol Soc       Date:  1992

2.  A fifth locus for Bardet-Biedl syndrome maps to chromosome 2q31.

Authors:  T L Young; L Penney; M O Woods; P S Parfrey; J S Green; D Hefferton; W S Davidson
Journal:  Am J Hum Genet       Date:  1999-03       Impact factor: 11.025

3.  Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families.

Authors:  R Fujita; M Buraczynska; L Gieser; W Wu; P Forsythe; M Abrahamson; S G Jacobson; P A Sieving; S Andréasson; A Swaroop
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

4.  A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3.

Authors:  R Fujita; E Bingham; P Forsythe; C McHenry; V Aita; B A Navia; K Dry; M Segal; M Devoto; G Bruns; A F Wright; J Ott; P A Sieving; A Swaroop
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

5.  RP2 phenotype and pathogenetic correlations in X-linked retinitis pigmentosa.

Authors:  Thiran Jayasundera; Kari E H Branham; Mohammad Othman; William R Rhoades; Athanasios J Karoukis; Hemant Khanna; Anand Swaroop; John R Heckenlively
Journal:  Arch Ophthalmol       Date:  2010-07

6.  Genetic analysis of Chinese families reveals a novel truncation allele of the retinitis pigmentosa GTPase regulator gene.

Authors:  Fang Hu; Xiang-Yun Zeng; Lin-Lin Liu; Yao-Ling Luo; Yi-Ping Jiang; Hui Wang; Jing Xie; Cheng-Quan Hu; Lin Gan; Liang Huang
Journal:  Int J Ophthalmol       Date:  2014-10-18       Impact factor: 1.779

Review 7.  Genetic characterization and disease mechanism of retinitis pigmentosa; current scenario.

Authors:  Muhammad Umar Ali; Muhammad Saif Ur Rahman; Jiang Cao; Ping Xi Yuan
Journal:  3 Biotech       Date:  2017-07-18       Impact factor: 2.406

8.  A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27.

Authors:  L Gieser; R Fujita; H H Göring; J Ott; D R Hoffman; A V Cideciyan; D G Birch; S G Jacobson; A Swaroop
Journal:  Am J Hum Genet       Date:  1998-11       Impact factor: 11.025

9.  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

10.  Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease.

Authors:  Kari Branham; Mohammad Othman; Matthew Brumm; Athanasios J Karoukis; Pelin Atmaca-Sonmez; Beverly M Yashar; Sharon B Schwartz; Niamh B Stover; Karmen Trzupek; Dianna Wheaton; Barbara Jennings; Maria Laura Ciccarelli; K Thiran Jayasundera; Richard A Lewis; David Birch; Jean Bennett; Paul A Sieving; Sten Andreasson; Jacque L Duncan; Gerald A Fishman; Alessandro Iannaccone; Richard G Weleber; Samuel G Jacobson; John R Heckenlively; Anand Swaroop
Journal:  Invest Ophthalmol Vis Sci       Date:  2012-12-13       Impact factor: 4.799

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.