Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases

BACKGROUND: Inherited retinal disorders are clinically and genetically heterogeneous with more than 150 gene defects accounting for the diversity of disease phenotypes. So far, mutation detection was mainly performed by APEX technology and direct Sanger sequencing of known genes. However, these meth...

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Detalles Bibliográficos
Autores principales: Audo, Isabelle, Bujakowska, Kinga M, Léveillard, Thierry, Mohand-Saïd, Saddek, Lancelot, Marie-Elise, Germain, Aurore, Antonio, Aline, Michiels, Christelle, Saraiva, Jean-Paul, Letexier, Mélanie, Sahel, José-Alain, Bhattacharya, Shomi S, Zeitz, Christina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352121/
https://www.ncbi.nlm.nih.gov/pubmed/22277662
http://dx.doi.org/10.1186/1750-1172-7-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352121/
https://www.ncbi.nlm.nih.gov/pubmed/22277662
http://dx.doi.org/10.1186/1750-1172-7-8

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