Literature DB >> 8513323

A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p.

C F Inglehearn1, S A Carter, T J Keen, J Lindsey, A M Stephenson, R Bashir, M al-Maghtheh, A T Moore, M Jay, A C Bird.   

Abstract

Autosomal dominant retinitis pigmentosa (adRP) is known to result from mutations in two different retinal genes--rhodopsin and peripherin--while a third locus has been implicated by linkage data. However, families have been reported in which all three known loci have been excluded. We report linkage of adRP in one such family to two microsatellite markers on chromosome 7p. D7S435 has previously been localized to 7p13-15.1; D7S460, previously only localized to chromosome 7, maps to within 2 cM of D7S435 with a lod score of 12.15. Two point linkage analysis between these markers and adRP gave lod scores of 5.65 (theta = 0) and 4.19 (theta = 0.046) for D7S460 and D7S435, respectively. Multipoint analysis gave a maximum lod score of 8.22. These data strongly suggest a new adRP locus on chromosome 7p.

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Year:  1993        PMID: 8513323     DOI: 10.1038/ng0593-51

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  25 in total

Review 1.  Pre-mRNA splicing and retinitis pigmentosa.

Authors:  Daniel Mordes; Xiaoyan Luo; Amar Kar; David Kuo; Lili Xu; Kazuo Fushimi; Guowu Yu; Paul Sternberg; Jane Y Wu
Journal:  Mol Vis       Date:  2006-10-26       Impact factor: 2.367

2.  Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele.

Authors:  T L McGee; M Devoto; J Ott; E L Berson; T P Dryja
Journal:  Am J Hum Genet       Date:  1997-11       Impact factor: 11.025

3.  Genetic modifiers of retinal degeneration in the rd3 mouse.

Authors:  Michael Danciger; Diego Ogando; Haidong Yang; Michael T Matthes; Nicole Yu; Kelly Ahern; Douglas Yasumura; Robert W Williams; Matthew M Lavail
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-03-14       Impact factor: 4.799

4.  Ophthalmic genetics: a genealogical guide to sources in England and Wales.

Authors:  M Jay
Journal:  J Med Genet       Date:  1995-12       Impact factor: 6.318

5.  Exclusion of CAG repeat expansion as the cause of disease in autosomal dominant retinitis pigmentosa families.

Authors:  T J Keen; A G Morris; C F Inglehearn
Journal:  J Med Genet       Date:  1997-02       Impact factor: 6.318

6.  RP11 is the second most common locus for dominant retinitis pigmentosa.

Authors:  E Vithana; M Al-Maghtheh; S S Bhattacharya; C F Inglehearn
Journal:  J Med Genet       Date:  1998-02       Impact factor: 6.318

7.  Phenotypic characterization of a large family with RP10 autosomal-dominant retinitis pigmentosa: an Asp226Asn mutation in the IMPDH1 gene.

Authors:  Petra Kozma; Dianna K Hughbanks-Wheaton; Kirsten G Locke; Garry E Fish; Anisa I Gire; Catherine J Spellicy; Lori S Sullivan; Sara J Bowne; Stephen P Daiger; David G Birch
Journal:  Am J Ophthalmol       Date:  2005-10-07       Impact factor: 5.258

8.  Dominant cystoid macular dystrophy associated with mutations in the RP1L1 gene.

Authors:  Yan Fu; Tian-Hao Xie; Yue-Ling Zhang; Na Yang; Xiao-Nan Shi; Zhao-Hui Gu
Journal:  Int J Ophthalmol       Date:  2019-12-18       Impact factor: 1.779

9.  Fine localization of the locus for autosomal dominant retinitis pigmentosa on chromosome 17p.

Authors:  R Goliath; Y Shugart; P Janssens; J Weissenbach; P Beighton; R Ramasar; J Greenberg
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

Review 10.  The genetic contribution to the phenotype.

Authors:  U Wolf
Journal:  Hum Genet       Date:  1995-02       Impact factor: 4.132

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