Literature DB >> 7509310

394delTT: a Nordic cystic fibrosis mutation.

M Schwartz1, M Anvret, M Claustres, H G Eiken, K Eiklid, C Schaedel, L Stolpe, L Tranebjaerg.   

Abstract

In a systematic screening for mutations in the gene encoding the cystic fibrosis transmembrane regulator among Danish cystic fibrosis (CF) patients, we identified a mutation in exon 3 (394delTT); this mutation was found to be relatively common in Denmark. We therefore screened for 394delTT in Sweden and Norway, where it turned out to be the second most frequent mutation, accounting for 4% of all CF mutations. It also occurs with a high frequency in Finland, but has not been found in larger surveys of mutations in the CFTR gene. Thus, 394delTT seems to be a specific Nordic CF mutation.

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Year:  1994        PMID: 7509310     DOI: 10.1007/bf00210602

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  25 in total

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Authors:  D Abeliovich; I P Lavon; I Lerer; T Cohen; C Springer; A Avital; G R Cutting
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

2.  Frequency of the delta F508 mutation on cystic fibrosis chromosomes in Denmark.

Authors:  M Schwartz; H K Johansen; C Koch; N J Brandt
Journal:  Hum Genet       Date:  1990-09       Impact factor: 4.132

3.  Genetic evidence for the spread of agriculture in Europe by demic diffusion.

Authors:  R R Sokal; N L Oden; C Wilson
Journal:  Nature       Date:  1991-05-09       Impact factor: 49.962

4.  Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction.

Authors:  M Orita; Y Suzuki; T Sekiya; K Hayashi
Journal:  Genomics       Date:  1989-11       Impact factor: 5.736

5.  Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locus.

Authors:  U B Gyllensten; H A Erlich
Journal:  Proc Natl Acad Sci U S A       Date:  1988-10       Impact factor: 11.205

6.  Frequency of four cystic fibrosis mutations in a Swedish population.

Authors:  N Dahl; U Grandell; T Martinsson; M Allen; L Johansson; L Stolpe; U Gyllensten; L Hjelte; H Kollberg; B Strandvik
Journal:  Acta Paediatr       Date:  1993 Jun-Jul       Impact factor: 2.299

7.  CA/GT microsatellite alleles within the cystic fibrosis transmembrane conductance regulator (CFTR) gene are not generated by unequal crossingover.

Authors:  N Morral; V Nunes; T Casals; X Estivill
Journal:  Genomics       Date:  1991-07       Impact factor: 5.736

8.  Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

Authors:  J Zielenski; R Rozmahel; D Bozon; B Kerem; Z Grzelczak; J R Riordan; J Rommens; L C Tsui
Journal:  Genomics       Date:  1991-05       Impact factor: 5.736

Review 9.  The spectrum of cystic fibrosis mutations.

Authors:  L C Tsui
Journal:  Trends Genet       Date:  1992-11       Impact factor: 11.639

10.  Incidence and survival curves of cystic fibrosis in Sweden.

Authors:  H Kollberg
Journal:  Acta Paediatr Scand       Date:  1982-03
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  3 in total

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Authors:  H B Eggesbø; S Søvik; S Dølvik; K Eiklid; F Kolmannskog
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2.  Assessing the Disease-Liability of Mutations in CFTR.

Authors:  Claude Ferec; Garry R Cutting
Journal:  Cold Spring Harb Perspect Med       Date:  2012-12-01       Impact factor: 6.915

3.  Cystic fibrosis in a low-incidence population: two major mutations in Finland.

Authors:  J Kere; X Estivill; M Chillón; N Morral; V Nunes; R Norio; E Savilahti; A de la Chapelle
Journal:  Hum Genet       Date:  1994-02       Impact factor: 4.132

  3 in total

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