Literature DB >> 1370875

Cystic fibrosis in the Basque country: high frequency of mutation delta F508 in patients of Basque origin.

T Casals1, C Vázquez, C Lázaro, E Girbau, F J Giménez, X Estivill.   

Abstract

The Basque population is one of the oldest populations of Europe. It has been suggested that the Basques arose from a population established in western Europe during the late Paleolithic Age. The Basque language (Euskera) is a supposedly pre-Indo-European language that originates from the first settlers of Europe. The variable distribution of the major cystic fibrosis (CF) mutation (delta F508 deletion) in Europe, with higher frequencies of the mutation in northern Europe and lower frequencies in southern Europe, has suggested that the delta F508 mutation was spread by early farmers migrating from the Middle East during the Neolithic period. We have studied 45 CF families from the Basque Country, where the incidence of CF is approximately 1/4,500. The birthplaces of the parents and grandparents have been traced and are distributed according to their origin as Basque or Mixed Basque. The frequency of the delta F508 mutation in the chromosomes of Basque origin is 87%, compared with 58% in those of Mixed Basque origin. The analysis of haplotypes, both with markers closely linked to the CF gene and with intragenic markers, suggests that the delta F508 mutation was not spread by the Indo-European invasions but was already present in Europe more than 10,000 years ago, during the Paleolithic period.

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Year:  1992        PMID: 1370875      PMCID: PMC1682450     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  28 in total

1.  The incidence of delta F508 CF mutation, and associated haplotypes, in a sample of English CF families.

Authors:  E K Watson; E S Mayall; L Simova; E M Thompson; J O Warner; R Williamson; C Williams
Journal:  Hum Genet       Date:  1990-09       Impact factor: 4.132

2.  Polymorphic DNA haplotypes and delta F508 deletion in 212 Italian CF families.

Authors:  G Novelli; P Gasparini; A Savoia; P F Pignatti; F Sangiuolo; B Dallapiccola
Journal:  Hum Genet       Date:  1990-09       Impact factor: 4.132

3.  Some red cell enzymes and haptoglobin gene frequencies in two Basque regions and León.

Authors:  M M de Pancorbo; L I Mazón; C de la Rica; A Vicario; C M Lostao
Journal:  Ann Hum Biol       Date:  1989 Mar-Apr       Impact factor: 1.533

4.  Mutation analysis for heterozygote detection and the prenatal diagnosis of cystic fibrosis.

Authors:  W K Lemna; G L Feldman; B Kerem; S D Fernbach; E P Zevkovich; W E O'Brien; J R Riordan; F S Collins; L C Tsui; A L Beaudet
Journal:  N Engl J Med       Date:  1990-02-01       Impact factor: 91.245

5.  DNA amplification for detection of the XV-2c polymorphism linked to cystic fibrosis.

Authors:  C L Rosenbloom; B S Kerem; J M Rommens; L C Tsui; B Wainwright; R Williamson; W E O'Brien; A L Beaudet
Journal:  Nucleic Acids Res       Date:  1989-09-12       Impact factor: 16.971

Review 6.  AK1, PGD, GC and HP frequencies in the Basque population: a review.

Authors:  A I Aguirre; A Vicario; L I Mazón; M M De Pancorbo; P Arizti; A Estomba; C M Lostao
Journal:  Gene Geogr       Date:  1989-04

7.  Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase.

Authors:  R K Saiki; D H Gelfand; S Stoffel; S J Scharf; R Higuchi; G T Horn; K B Mullis; H A Erlich
Journal:  Science       Date:  1988-01-29       Impact factor: 47.728

8.  Cystic fibrosis mutation delta F508 in Finland: other mutations predominate.

Authors:  J Kere; E Savilahti; R Norio; X Estivill; A de la Chapelle
Journal:  Hum Genet       Date:  1990-09       Impact factor: 4.132

9.  Reconstruction of human evolution: bringing together genetic, archaeological, and linguistic data.

Authors:  L L Cavalli-Sforza; A Piazza; P Menozzi; J Mountain
Journal:  Proc Natl Acad Sci U S A       Date:  1988-08       Impact factor: 11.205

10.  Identification of the cystic fibrosis gene: chromosome walking and jumping.

Authors:  J M Rommens; M C Iannuzzi; B Kerem; M L Drumm; G Melmer; M Dean; R Rozmahel; J L Cole; D Kennedy; N Hidaka
Journal:  Science       Date:  1989-09-08       Impact factor: 47.728

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  8 in total

1.  An ancient founder mutation in PROKR2 impairs human reproduction.

Authors:  Magdalena Avbelj Stefanija; Marc Jeanpierre; Gerasimos P Sykiotis; Jacques Young; Richard Quinton; Ana Paula Abreu; Lacey Plummer; Margaret G Au; Ravikumar Balasubramanian; Andrew A Dwyer; Jose C Florez; Timothy Cheetham; Simon H Pearce; Radhika Purushothaman; Albert Schinzel; Michel Pugeat; Elka E Jacobson-Dickman; Svetlana Ten; Ana Claudia Latronico; James F Gusella; Catherine Dode; William F Crowley; Nelly Pitteloud
Journal:  Hum Mol Genet       Date:  2012-07-05       Impact factor: 6.150

2.  Analysis of the CFTR gene confirms the high genetic heterogeneity of the Spanish population: 43 mutations account for only 78% of CF chromosomes.

Authors:  M Chillón; T Casals; J Giménez; M D Ramos; A Palacio; N Morral; X Estivill; V Nunes
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

3.  Cystic fibrosis in Spain: high frequency of mutation G542X in the Mediterranean coastal area.

Authors:  T Casals; V Nunes; A Palacio; J Giménez; A Gaona; N Ibáñez; N Morral; X Estivill
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

4.  Prevalence of cystic fibrosis mutations in the Grampian region of Scotland.

Authors:  Z H Miedzybrodzka; J C Dean; G Russell; J A Friend; K F Kelly; N E Haites
Journal:  J Med Genet       Date:  1993-04       Impact factor: 6.318

5.  Analysis of the genotypic profile and its relationship with the clinical manifestations in people with cystic fibrosis: study from a rare disease registry.

Authors:  Senay Rueda-Nieto; Pedro Mondejar-Lopez; María-Pilar Mira-Escolano; Ana Cutillas-Tolín; Luis Alberto Maceda-Roldán; Julián Jesús Arense-Gonzalo; Joaquín A Palomar-Rodríguez
Journal:  Orphanet J Rare Dis       Date:  2022-06-13       Impact factor: 4.303

6.  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

7.  Population specificity of the DNAI1 gene mutation spectrum in primary ciliary dyskinesia (PCD).

Authors:  Ewa Ziętkiewicz; Barbara Nitka; Katarzyna Voelkel; Urszula Skrzypczak; Zuzanna Bukowy; Ewa Rutkiewicz; Kinga Humińska; Hanna Przystałowska; Andrzej Pogorzelski; Michał Witt
Journal:  Respir Res       Date:  2010-12-08

8.  Identification and selection of healthy spermatozoa in heterozygous carriers of the Phe508del-variant of the CFTR-gene in assisted reproduction.

Authors:  Julie De Geyter; Sabina Gallati-Kraemer; Hong Zhang; Christian De Geyter
Journal:  Sci Rep       Date:  2022-02-03       Impact factor: 4.996

  8 in total

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