Napredna pretraga

Pregled bibliografske jedinice broj: 88533

The occurrence of the most common CFTR mutations among Croatian cystic fibrosis patients


Tanacković, Goranka; Barišić, Ingeborg; Pavelić, Krešimir
The occurrence of the most common CFTR mutations among Croatian cystic fibrosis patients // European Journal of Human Genetics, 7 (1999), Suppl 1. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)


Naslov
The occurrence of the most common CFTR mutations among Croatian cystic fibrosis patients

Autori
Tanacković, Goranka ; Barišić, Ingeborg ; Pavelić, Krešimir

Izvornik
European Journal of Human Genetics (1018-4813) 7 (1999), Suppl 1;

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, kongresno priopcenje, znanstveni

Ključne riječi
Cystic fibrosis; mutations; prevalence

Sažetak
Cystic fibrosis is the most common recessive disorder caused by mutations in the Cystic Fibrosis Transmembrane Conductance Regulator gene (CFTR). Over 700 different mutations within the CFTR gene have been reported, and their distribution depends on ethnic and geographic origin of CF patients. Most of the nations in Europe have identified their major CF mutations and so already established CF screening programme. Since there is no much data concerning the CFTR mutations among cystic fibrosis patients of Croatian origin, the aim of our study was to identify the most common mutations and to create CF screening programme that would enable a complete CF mutation detection among our patietns. To obtain this we studied the 16 most frequent CF mutations ; DF508, G542X, G551D, W1282X, 3905insT, N1303K, 3849+10kbC--T, R553X, 621+1G--, 1717-1G--A, 2789+5G--A, 3849+4A--G, R1162X, 1898*1G--A, R117H and DI507 (issued by CF Genetic Analysis Consortium). Wa also used DGGE method for exons 3, 4, 7, 10, 11, 13, 19 and 20 to find some other mutations. The result of molecular analysis of 66 CF chromosome revealed the following frequency of detected mutations: DF508 (62%), G542 (7, 6%), N1303K (3%), G85E (3%), 1717-1G--A (3%), R117H (3%), and R1162X (1.5%). In the two families the polymorphism P1290P was found. Since 16.9% of CF alleles in this study were yet unidentified, furtehr analyisis is planed, including screening for nes mutations and DNA sequencing.

Izvorni jezik
Engleski

Znanstvena područja
Biologija



POVEZANOST RADA


Projekt / tema
072777

Ustanove
Klinika za dječje bolesti Medicinskog fakulteta

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


Uključenost u ostale bibliografske baze podataka:


  • Excerpta Medica
  • Index Medicus