Literature DB >> 11910130

Mutation analysis of codons 345 and 347 of rhodopsin gene in Indian retinitis pigmentosa patients.

M Dikshit1, R Agarwal.   

Abstract

More than 100 mutations have been reported till date in the rhodopsin gene in patients with retinitis pigmentosa. The present study was undertaken to detect the reported rhodopsin gene point mutations in Indian retinitis pigmentosa patients. We looked for presence or absence of codon 345 and 347 mutations in exon 5 of the gene using the technique of allele-specific polymerase chain reaction by designing primers for each mutation. We have examined 100 patients from 76 families irrespective of genetic categories. Surprisingly, in our sample the very widely reported highly frequent mutations of codon 347 (P --> S/A/R/Q/L/T) were absent while the codon 345 mutation V --> M was seen in three cases in one family (autosomal dominant form) and in one sporadic case (total two families). This is the first report on codon 345 and 347 mutation in Indian retinitis pigmentosa subjects.

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Year:  2001        PMID: 11910130     DOI: 10.1007/BF02728336

Source DB:  PubMed          Journal:  J Genet        ISSN: 0022-1333            Impact factor:   1.508


  29 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-01       Impact factor: 11.205

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Authors:  M Nakazawa; E Kikawa-Araki; T Shiono; M Tamai
Journal:  Jpn J Ophthalmol       Date:  1991       Impact factor: 2.447

5.  Further screening of the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.

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Journal:  Genomics       Date:  1994-05-15       Impact factor: 5.736

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Journal:  Proc Natl Acad Sci U S A       Date:  1995-03-28       Impact factor: 11.205

7.  Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (ADRP).

Authors:  K Fujiki; Y Hotta; M Hayakawa; H Sakuma; T Shiono; M Noro; T Sakuma; M Tamai; K Hikiji; R Kawaguchi
Journal:  Jpn J Hum Genet       Date:  1992-06

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Authors:  M Nakazawa
Journal:  Nippon Ganka Gakkai Zasshi       Date:  1993-12

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Authors:  E L Berson; J F Remulla; B Rosner; M A Sandberg; C Weigel-DiFranco
Journal:  Arch Ophthalmol       Date:  1996-05
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  5 in total

Review 1.  Finding and interpreting genetic variations that are important to ophthalmologists.

Authors:  Edwin M Stone
Journal:  Trans Am Ophthalmol Soc       Date:  2003

2.  Retinal histopathology in eyes from patients with autosomal dominant retinitis pigmentosa caused by rhodopsin mutations.

Authors:  Vera L Bonilha; Mary E Rayborn; Brent A Bell; Meghan J Marino; Craig D Beight; Gayle J Pauer; Elias I Traboulsi; Joe G Hollyfield; Stephanie A Hagstrom
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2015-07-23       Impact factor: 3.117

Review 3.  Genetics of Inherited Retinal Diseases in Understudied Populations.

Authors:  Chitra Kannabiran; Deepika Parameswarappa; Subhadra Jalali
Journal:  Front Genet       Date:  2022-02-28       Impact factor: 4.599

4.  Identification of two mutations of the RHO gene in two Chinese families with retinitis pigmentosa: correlation between genotype and phenotype.

Authors:  Zhe Pan; Tingting Lu; Xiaohui Zhang; Hanjun Dai; Weiyu Yan; Fengge Bai; Yang Li
Journal:  Mol Vis       Date:  2012-12-14       Impact factor: 2.367

5.  Retinitis pigmentosa: mutation analysis of RHO, PRPF31, RP1, and IMPDH1 genes in patients from India.

Authors:  Mamatha Gandra; Venkataramana Anandula; Vidhya Authiappan; Srilekha Sundaramurthy; Rajiv Raman; Shomi Bhattacharya; Kumaramanickavel Govindasamy
Journal:  Mol Vis       Date:  2008-06-14       Impact factor: 2.367

  5 in total

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