## Communicated by Randy Eisensmith Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene cause cystic fibrosis (CF), a common autosomal recessive disease in Caucasians. The broad mutation spectrum varies among different patient groups. Current molecular diagnoses are de
✦ LIBER ✦
Detection of 100% of the CFTR mutations in 63 CF families from Tyrol
✍ Scribed by M. Stuhrmann; T. Dörk; M. Frühwirth; A. Golla; B. Skawran; W. Antonin; M. Ebhardt; A. Loos; H. Ellemunter; J. Schmidtke
- Book ID
- 110887684
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 879 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0009-9163
No coin nor oath required. For personal study only.
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