Identification of the Photoreceptor Transcriptional Co-Repressor SAMD11 as Novel Cause of Autosomal Recessive Retinitis Pigmentosa

Retinitis pigmentosa (RP), the most frequent form of inherited retinal dystrophy is characterized by progressive photoreceptor degeneration. Many genes have been implicated in RP development, but several others remain to be identified. Using a combination of homozygosity mapping, whole-exome and tar...

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Detalles Bibliográficos
Autores principales: Corton, M., Avila-Fernández, A., Campello, L., Sánchez, M., Benavides, B., López-Molina, M. I., Fernández-Sánchez, L., Sánchez-Alcudia, R., da Silva, L. R. J., Reyes, N., Martín-Garrido, E., Zurita, O., Fernández-San José, P., Pérez-Carro, R., García-García, F., Dopazo, J., García-Sandoval, B., Cuenca, N., Ayuso, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062157/
https://www.ncbi.nlm.nih.gov/pubmed/27734943
http://dx.doi.org/10.1038/srep35370

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062157/
https://www.ncbi.nlm.nih.gov/pubmed/27734943
http://dx.doi.org/10.1038/srep35370

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