An appropriate diagnostic approach can improve detection of CFTR mutations: the experience in Patients with Classical Form of Cystic Fibrosis coming from an Italian Region with high genetic heterogeneity

✍ Scribed by A. Ravani; A. Venturoli; S. Carturan; S. Brioschi; M. Taddei Masieri; S. Fini; C. Trabanelli; B. Dolcini; P. Rimessi; F. Battistini; M. Ambroni; G.L. Grzincich; E. Calzolari; A. Ferlini

• Book ID: 118642035
• Publisher: Elsevier Science
• Year: 2009
• Tongue: English
• Weight: 57 KB
• Volume: 8
• Category: Article
• ISSN: 1569-1993
• DOI: 10.1016/s1569-1993(09)60029-1