Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) gene
Year: 1992
Type: article
Study design: Observational Study
Source: Human Genetics
DOI: 10.1007/bf00221957
Authors: L. Osborne, G. Santis, M. Schwarz, K. Klinger, T. Dörk, I. McIntosh, M. Schwartz, V. Nunes, M. Macek, J. Reiss, W. E. Highsmith, R. McMahon, G. Novelli, N. Malik, J. Bürger, M. Anvret, A. Wallace, C. Williams, C. Mathew, R. Rozen, C. Graham, P. Gasparini, J. Bal, J. J. Cassiman, A. Balassopoulou, L. Davidow, S. Raskin, L. Kalaydjieva, B. Kerem, S. Richards, B. Simon-Bouy, M. Super, U. Wulbrand, M. Keston, X. Estivill, V. Vavrova, K. J. Friedman, D. Barton, B. Dallapiccola, M. Stuhrmann, F. Beards, A. J. M. Hill, P. F. Pignatti, H. Cuppens, D. Angelicheva, B. Tümmler, D. J. H. Brock, T. Casals, M. Macek, J. Schmidtke, A. C. Magee, A. Bonizzato, C. De Boeck, A. Kuffardjieva, M. Hodson, R. A. Knight
Institutions: Royal Manchester Children's Hospital, Sequenom (United States), Medizinische Hochschule Hannover, Western General Hospital, University of Edinburgh, University of Copenhagen, Rigshospitalet, Duran i Reynals Hospital, Charles University, Freie Universität Berlin, University of Göttingen, University of Cambridge, University of Urbino, Karolinska University Hospital, St Mary's Hospital, St Mary's Hospital, Montreal Children's Hospital, McGill University, Belfast City Hospital, University of Verona, KU Leuven, National and Kapodistrian University of Athens, Vanderbilt University Medical Center, Hebrew University of Jerusalem, Inserm, Château de Longchamp
Language: English
Subfield: Pulmonary and Respiratory Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2028859322