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

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Title: Targeted Next Generation Sequencing Identifies Novel Mutations in RP1 as a Relatively Common Cause of Autosomal Recessive Rod-Cone Dystrophy.
Authors: El Shamieh, Said1,2,3 said.elshamieh@inserm.fr, Boulanger-Scemama, Elise1,2,3 boulanger.el@gmail.com, Lancelot, Marie-Elise1,2,3 marie-elise.lancelot@laposte.net, Antonio, Aline1,2,3 aline.antonio@inserm.fr, Démontant, Vanessa1,2,3 vanessa.demontant@inserm.fr, Condroyer, Christel1,2,3 christel.condroyer@inserm.fr, Letexier, Mélanie4 melanie.letexier@integragen.com, Saraiva, Jean-Paul4 jean-paul.saraiva@integragen.com, Mohand-Saïd, Saddek1,2,3,5 saddekms@gmail.com, Sahel, José-Alain1,2,3,5,6,7,8 j.sahel@gmail.com, Audo, Isabelle1,2,3,5,8 isabelle.audo@inserm.fr, Zeitz, Christina1,2,3 christina.zeitz@inserm.fr
Source: BioMed Research International. 1/6/2015, Vol. 2015, p1-11. 11p.
Database: Academic Search Ultimate
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  Data: Targeted Next Generation Sequencing Identifies Novel Mutations in RP1 as a Relatively Common Cause of Autosomal Recessive Rod-Cone Dystrophy.
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  Data: <searchLink fieldCode="AR" term="%22El+Shamieh%2C+Said%22">El Shamieh, Said</searchLink><relatesTo>1,2,3</relatesTo><i> said.elshamieh@inserm.fr</i><br /><searchLink fieldCode="AR" term="%22Boulanger-Scemama%2C+Elise%22">Boulanger-Scemama, Elise</searchLink><relatesTo>1,2,3</relatesTo><i> boulanger.el@gmail.com</i><br /><searchLink fieldCode="AR" term="%22Lancelot%2C+Marie-Elise%22">Lancelot, Marie-Elise</searchLink><relatesTo>1,2,3</relatesTo><i> marie-elise.lancelot@laposte.net</i><br /><searchLink fieldCode="AR" term="%22Antonio%2C+Aline%22">Antonio, Aline</searchLink><relatesTo>1,2,3</relatesTo><i> aline.antonio@inserm.fr</i><br /><searchLink fieldCode="AR" term="%22Démontant%2C+Vanessa%22">Démontant, Vanessa</searchLink><relatesTo>1,2,3</relatesTo><i> vanessa.demontant@inserm.fr</i><br /><searchLink fieldCode="AR" term="%22Condroyer%2C+Christel%22">Condroyer, Christel</searchLink><relatesTo>1,2,3</relatesTo><i> christel.condroyer@inserm.fr</i><br /><searchLink fieldCode="AR" term="%22Letexier%2C+Mélanie%22">Letexier, Mélanie</searchLink><relatesTo>4</relatesTo><i> melanie.letexier@integragen.com</i><br /><searchLink fieldCode="AR" term="%22Saraiva%2C+Jean-Paul%22">Saraiva, Jean-Paul</searchLink><relatesTo>4</relatesTo><i> jean-paul.saraiva@integragen.com</i><br /><searchLink fieldCode="AR" term="%22Mohand-Saïd%2C+Saddek%22">Mohand-Saïd, Saddek</searchLink><relatesTo>1,2,3,5</relatesTo><i> saddekms@gmail.com</i><br /><searchLink fieldCode="AR" term="%22Sahel%2C+José-Alain%22">Sahel, José-Alain</searchLink><relatesTo>1,2,3,5,6,7,8</relatesTo><i> j.sahel@gmail.com</i><br /><searchLink fieldCode="AR" term="%22Audo%2C+Isabelle%22">Audo, Isabelle</searchLink><relatesTo>1,2,3,5,8</relatesTo><i> isabelle.audo@inserm.fr</i><br /><searchLink fieldCode="AR" term="%22Zeitz%2C+Christina%22">Zeitz, Christina</searchLink><relatesTo>1,2,3</relatesTo><i> christina.zeitz@inserm.fr</i>
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  Data: <searchLink fieldCode="JN" term="%22BioMed+Research+International%22">BioMed Research International</searchLink>. 1/6/2015, Vol. 2015, p1-11. 11p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=109273038
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