Analysis of a sample of 50 unrelated cystic fibrosis (CF) patients and 46 nuclear families from Slovakia (Czechoslovakia) by the polymerase chain reaction and Southern hybridization revealed that the proportion of the delta F508 mutation was 58% in this population, and that the frequency of the B (i.e., KM19/XV2c [1-2]) haplotype was increased in both delta F508 and non-delta F508 CF chromosomes (98% and 46%, respectively). These results support the view that the trans-European gradient of the delta F508 frequency is of a geographical rather than of an ethnic origin, and that in Slavonic populations, there exists an as yet unidentified but frequent CF mutation other than delta F508, associated with the B haplotype.

Deletion delta F508 and haplotype analysis of CFTR gene region in Slovak CF patients / L., Kadasi; J., Gecz; J., Matusek; T., Krivusova; V., Ferak; Devoto, Marcella; J., Hruskovic; G., Romeo. - In: HUMAN GENETICS. - ISSN 0340-6717. - 89:3(1992).

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

DEVOTO, MARCELLA;
1992

Abstract

Analysis of a sample of 50 unrelated cystic fibrosis (CF) patients and 46 nuclear families from Slovakia (Czechoslovakia) by the polymerase chain reaction and Southern hybridization revealed that the proportion of the delta F508 mutation was 58% in this population, and that the frequency of the B (i.e., KM19/XV2c [1-2]) haplotype was increased in both delta F508 and non-delta F508 CF chromosomes (98% and 46%, respectively). These results support the view that the trans-European gradient of the delta F508 frequency is of a geographical rather than of an ethnic origin, and that in Slavonic populations, there exists an as yet unidentified but frequent CF mutation other than delta F508, associated with the B haplotype.
1992
01 Pubblicazione su rivista::01a Articolo in rivista
Deletion delta F508 and haplotype analysis of CFTR gene region in Slovak CF patients / L., Kadasi; J., Gecz; J., Matusek; T., Krivusova; V., Ferak; Devoto, Marcella; J., Hruskovic; G., Romeo. - In: HUMAN GENETICS. - ISSN 0340-6717. - 89:3(1992).
File allegati a questo prodotto
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/497417
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? 1
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact