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

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Bibliographic Details
Title:	Targeted Next Generation Sequencing Identifies Novel Mutations in RP1 as a Relatively Common Cause of Autosomal Recessive Rod-Cone Dystrophy.
Authors:	El Shamieh, Said^1,2,3 said.elshamieh@inserm.fr, Boulanger-Scemama, Elise^1,2,3 boulanger.el@gmail.com, Lancelot, Marie-Elise^1,2,3 marie-elise.lancelot@laposte.net, Antonio, Aline^1,2,3 aline.antonio@inserm.fr, Démontant, Vanessa^1,2,3 vanessa.demontant@inserm.fr, Condroyer, Christel^1,2,3 christel.condroyer@inserm.fr, Letexier, Mélanie⁴ melanie.letexier@integragen.com, Saraiva, Jean-Paul⁴ jean-paul.saraiva@integragen.com, Mohand-Saïd, Saddek^1,2,3,5 saddekms@gmail.com, Sahel, José-Alain^{1,2,3,5,6,7,8} j.sahel@gmail.com, Audo, Isabelle^1,2,3,5,8 isabelle.audo@inserm.fr, Zeitz, Christina^1,2,3 christina.zeitz@inserm.fr
Source:	BioMed Research International. 1/6/2015, Vol. 2015, p1-11. 11p.
Database:	Academic Search Ultimate

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ISSN:	23146133
DOI:	10.1155/2015/485624