Nothing to declare
Extensive sequence analysis of CFTR, SCNN1A, SCNN1B, SCNN1G and SERPINA1 suggests an oligogenic basis for cystic fibrosis-like phenotypes
Article first published online: 28 JUL 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Special Issue: Personalized Medicine and Clinical Genetics
Volume 86, Issue 1, pages 91–95, July 2014
How to Cite
Ramos, M.D., Trujillano, D., Olivar, R., Sotillo, F., Ossowski, S., Manzanares, J., Costa, J., Gartner, S., Oliva, C., Quintana, E., Gonzalez, M.I., Vazquez, C., Estivill, X. and Casals, T. (2014), Extensive sequence analysis of CFTR, SCNN1A, SCNN1B, SCNN1G and SERPINA1 suggests an oligogenic basis for cystic fibrosis-like phenotypes. Clinical Genetics, 86: 91–95. doi: 10.1111/cge.12234
These authors equally contributed.
- Issue published online: 3 JUN 2014
- Article first published online: 28 JUL 2013
- Accepted manuscript online: 9 JUL 2013 12:25PM EST
- Manuscript Revised: 5 JUL 2013
- Manuscript Accepted: 5 JUL 2013
- Manuscript Received: 1 MAR 2013
- Spanish Plan Nacional (NOVADIS). Grant Number: SAF2008-00357
- Generalitat de Catalunya. Grant Number: AGAUR 2009 SGR-1502
- Instituto de Salud Carlos III. Grant Number: FIS/FEDER PI11/00733
- Federación Española de FQ
- GEUVADIS. Grant Number: 261123
- ESGI. Grant Number: 262055
- Spanish Ministry of Economy and Competiveness
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