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BioMed Research International
Volume 2015 (2015), Article ID 485624, 11 pages
http://dx.doi.org/10.1155/2015/485624
Research Article

Targeted Next Generation Sequencing Identifies Novel Mutations in RP1 as a Relatively Common Cause of Autosomal Recessive Rod-Cone Dystrophy

1INSERM, U968, 75012 Paris, France
2Sorbonne Universités, UPMC University, Paris 06, UMR_S 968, Institut de la Vision, 75012 Paris, France
3CNRS, UMR_7210, 75012 Paris, France
4IntegraGen SA, Genopole Campus 1, Building G8, 91030 Evry, France
5Centre Hospitalier National d’Ophtalmologie des Quinze-Vingts, DHU ViewMaintain, INSERM-DHOS CIC 1423, 75012 Paris, France
6Fondation Ophtalmologique Adolphe de Rothschild, 75019 Paris, France
7Académie des Sciences-Institut de France, 75006 Paris, France
8University College London Institute of Ophthalmology, 11-43 Bath Street, London EC1V 9EL, UK

Received 27 June 2014; Accepted 10 July 2014

Academic Editor: Calvin Yu-Chian Chen

Copyright © 2015 Said El Shamieh 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

Said El Shamieh, Elise Boulanger-Scemama, Marie-Elise Lancelot, et al., “Targeted Next Generation Sequencing Identifies Novel Mutations in RP1 as a Relatively Common Cause of Autosomal Recessive Rod-Cone Dystrophy,” BioMed Research International, vol. 2015, Article ID 485624, 11 pages, 2015. doi:10.1155/2015/485624