Whole-exome sequencing reveals ZNF408 as a new gene associated with autosomal recessive retinitis pigmentosa with vitreal alterations-Reference-Cited by-同舟云学术

Whole-exome sequencing reveals ZNF408 as a new gene associated with autosomal recessive retinitis pigmentosa with vitreal alterations

Published:2015-04-16 Issue:14 Volume:24 Page:4037-4048
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Avila-Fernandez Almudena,Perez-Carro Raquel,Corton Marta,Lopez-Molina Maria Isabel,Campello Laura,Garanto Alejandro,Fernandez-Sanchez Laura,Duijkers Lonneke,Lopez-Martinez Miguel Angel,Riveiro-Alvarez Rosa,Da Silva Luciana Rodrigues Jacy,Sanchez-Alcudia Rocío,Martin-Garrido Esther,Reyes Noelia,Garcia-Garcia Francisco,Dopazo Joaquin,Garcia-Sandoval Blanca,Collin Rob W.J.,Cuenca Nicolas,Ayuso Carmen

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/24/14/4037/17262158/ddv140.pdf

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4. Lighting a candle in the dark: advances in genetics and gene therapy of recessive retinal dystrophies;den Hollander;J. Clin. Invest,2010

5. Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait;Wright;Nat. Rev. Genet,2010

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