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Case Reports in Genetics
Volume 2014, Article ID 613863, 4 pages
http://dx.doi.org/10.1155/2014/613863
Case Report

Apparent Homozygosity of p.Phe508del in CFTR due to a Large Gene Deletion of Exons 4–11

1Department of Molecular Genetics, Function and Therapy, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, 1683 Nicosia, Cyprus
2Department of Pediatrics, Hospital “Archbishop Makarios III”, 1474 Nicosia, Cyprus
3Cyprus International Institute for Environmental & Public Health in Association with Harvard School of Public Health, Cyprus University of Technology, 95 Irenes Street, 3041 Limassol, Cyprus
4Department of Clinical Genetics, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, 1683 Nicosia, Cyprus
5Department of Cytogenetics and Genomics, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, 1683 Nicosia, Cyprus
6Translational Genomics Team, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, 1683 Nicosia, Cyprus

Received 22 November 2013; Accepted 23 December 2013; Published 6 February 2014

Academic Editors: S. Chappell, C.-W. Cheng, and G. Vogt

Copyright © 2014 Vassos Neocleous et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Vassos Neocleous, Panayiotis K. Yiallouros, George A. Tanteles, et al., “Apparent Homozygosity of p.Phe508del in CFTR due to a Large Gene Deletion of Exons 4–11,” Case Reports in Genetics, vol. 2014, Article ID 613863, 4 pages, 2014. https://doi.org/10.1155/2014/613863.