Literature DB >> 2210755

Frequency of the delta F508 mutation and flanking marker haplotypes at the CF locus from 167 Czech families.

M Macek1, V Vavrová, I Böhm, M Stuhrmann, A Reis, R Duspivová, M Macek1, K Sperling, M Krawczak, J Schmidtke.   

Abstract

This study analyses distribution patterns of the delta F508 mutation of the cystic fibrosis transmembrane conductance regulator gene (CFTR) gene and the cystic fibrosis (CF)-linked marker loci MET, D7S23, D7S399, and D7S8 in a sample of 167 (116 complete) CF families from Bohemia and Moravia (Czechoslovakia). DNA typing was performed by polymerase chain reaction amplification, restriction analysis, and agarose or polyacrylamide gel electrophoresis. The frequency of the delta F508 mutation in this sample is 67% and the frequency of the B haplotype is 77.6% on CF chromosomes. Linkage disequilibrium was found between delta F508 and all markers tested.

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Year:  1990        PMID: 2210755     DOI: 10.1007/bf02428289

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


  2 in total

1.  Deletion delta F508 and haplotype analysis of CFTR gene region in Slovak CF patients.

Authors:  L Kádasi; J Gécz; J Matúsek; T Krivusová; V Ferák; M Devoto; J Hruskovic; G Romeo
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

2.  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

  2 in total

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