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Cystic Fibrosis Mutations and Associated Haplotypes in Turkish Cystic Fibrosis Patients

TUNCER ONAY, JULIAN ZIELENSKI, OZLEM TOPALOGLU, NALAN GOKGOZ, HULYA KAYSERILI, MEMNUNE YUKSEL APAK, YILDIZ CAMCIOGLU, HALUK COKUGRAS, NECLA AKCAKAYA, LAP-CHEE TSUI and BETUL KIRDAR
Human Biology
Vol. 73, No. 2 (April 2001), pp. 191-203
Stable URL: http://www.jstor.org/stable/41465930
Page Count: 13
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Cystic Fibrosis Mutations and Associated Haplotypes in Turkish Cystic Fibrosis Patients
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Abstract

Identification of mutations causing cystic fibrosis (CF) in the Turkish population is essential for assessment of the molecular basis of CF in Turkey and the development of strategies for prenatal diagnosis and genetic counseling. Here, we present an updated report of mutations found in the Turkish CF population from an extensive screening study of the entire coding region, including exon-intron boundaries and the promoter region. Cases for which mutations could not be identified were also screened for previously defined large alterations and (TG)m Tn-M470V loci. This study revealed a total of 27 different mutations accounting for almost 60% of disease genes in the Turkish population. In this study, we also identified the haplotypes associated with 17 mutations and those associated with unknown mutations. The mutation spectrum of CF in Turkey and its associated haplotypes indicated the presence of a major Mediterranean component in the contemporary Turkish population.

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