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Cystic Fibrosis Gene Mutations ΔF508 and 394delTT in Patients with Chronic Sinusitis in Finland

✍ Scribed by Hytönen, Markku Patjas, Seija I. Ve, Maija

Book ID
120819042
Publisher
Informa plc
Year
2001
Tongue
English
Weight
107 KB
Volume
121
Category
Article
ISSN
0001-6489

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✍ María Roqué; Clara Pott Godoy; Mariana Castellanos; Eduardo Pusiol; Luis S. Mayo 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 35 KB

Cystic fibrosis (CF) is the most common autosomal recessive disease in the Caucasian population. The disease can be caused by one of the more than 900 different mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene. However, the deletion of the phe508-codon is the most pre