Literature DB >> 7512860

Identification of six novel mutations in the CFTR gene of patients from Bulgaria by screening the twenty seven exons and exon/intron boundaries using DGGE and direct DNA sequencing.

A Savov1, B Mercier, L Kalaydjieva, C Férec.   

Abstract

The CFTR gene, in which more than 300 mutations have been described, displays a spectrum of mutations which varies according to ethnic and geographic origin of patients. In this paper we report an exhaustive study of the 27 exons and exon/intron boundaries of a sample of 35 CF patients from Bulgaria which is situated in the south east of Europe. We have used denaturing gradient gel electrophoresis assay followed by DNA sequencing and we report the identification of six previously undescribed CFTR alleles.

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Year:  1994        PMID: 7512860     DOI: 10.1093/hmg/3.1.57

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  8 in total

1.  Analysis of the complete coding region of the CFTR gene in a cohort of CF patients from north-eastern Italy: identification of 90% of the mutations.

Authors:  A Bonizzato; L Bisceglia; C Marigo; E Nicolis; C Bombieri; C Castellani; G Borgo; L Zelante; G Mastella; G Cabrini
Journal:  Hum Genet       Date:  1995-04       Impact factor: 4.132

Review 2.  CFTR: domains, structure, and function.

Authors:  S Devidas; W B Guggino
Journal:  J Bioenerg Biomembr       Date:  1997-10       Impact factor: 2.945

3.  Comparison of the gating behaviour of human and murine cystic fibrosis transmembrane conductance regulator Cl- channels expressed in mammalian cells.

Authors:  K A Lansdell; S J Delaney; D P Lunn; S A Thomson; D N Sheppard; B J Wainwright
Journal:  J Physiol       Date:  1998-04-15       Impact factor: 5.182

4.  Effects of cystic fibrosis and congenital bilateral absence of the vas deferens-associated mutations on cystic fibrosis transmembrane conductance regulator-mediated regulation of separate channels.

Authors:  J E Mickle; M I Milewski; M Macek; G R Cutting
Journal:  Am J Hum Genet       Date:  2000-04-04       Impact factor: 11.025

5.  Localization studies of rare missense mutations in cystic fibrosis transmembrane conductance regulator (CFTR) facilitate interpretation of genotype-phenotype relationships.

Authors:  Kristina V Krasnov; Maria Tzetis; Jie Cheng; William B Guggino; Garry R Cutting
Journal:  Hum Mutat       Date:  2008-11       Impact factor: 4.878

6.  Independent origins of cystic fibrosis mutations R334W, R347P, R1162X, and 3849 + 10kbC-->T provide evidence of mutation recurrence in the CFTR gene.

Authors:  N Morral; R Llevadot; T Casals; P Gasparini; M Macek; T Dörk; X Estivill
Journal:  Am J Hum Genet       Date:  1994-11       Impact factor: 11.025

7.  Mutation analysis in 600 French cystic fibrosis patients.

Authors:  F Chevalier-Porst; A M Bonardot; R Gilly; J P Chazalette; M Mathieu; D Bozon
Journal:  J Med Genet       Date:  1994-07       Impact factor: 6.318

8.  A cluster of cystic fibrosis mutations in exon 17b of the CFTR gene: a site for rare mutations.

Authors:  B Mercier; W Lissens; G Novelli; L Kalaydjieva; M de Arce; N Kapranov; N Canki Klain; X Estivill; A Palacio; S Cashman
Journal:  J Med Genet       Date:  1994-09       Impact factor: 6.318

  8 in total

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