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Frequency of the F508 deletion in the CFTR gene in Turkish cystic fibrosis patients

✍ Scribed by Joachim Hundrieser; Silvia Bremer; Frank Peinemann; Manfred Stuhrmann; Nicola Hoffknecht; Brigitte Wulf; Jörg Schmidtke; Jochen Reiss; Günter Maaß; Burkhard Tümmler


Publisher
Springer
Year
1990
Tongue
English
Weight
188 KB
Volume
85
Category
Article
ISSN
0340-6717

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The occurrence of various non-ΔF508 CFTR
✍ Margit Nemeti; John P. Johnson; Zoltan Papp; Elaine Louie 📂 Article 📅 1992 🏛 Springer 🌐 English ⚖ 227 KB

Cystic fibrosis (CF) is an autosomal recessive disease caused by different mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The frequency of the major mutation (delta F508) in the Hungarian population is 64%. To identify other common mutations in CF families from Hun