Cargando…
Genes Associated with Retinitis Pigmentosa and Allied Diseases Are Frequently Mutated in the General Population
BACKGROUND: Retinitis pigmentosa and other hereditary retinal degenerations (HRD) are rare genetic diseases leading to progressive blindness. Recessive HRD are caused by mutations in more than 100 different genes. Laws of population genetics predict that, on a purely theoretical ground, such a high...
Autores principales: | Nishiguchi, Koji M., Rivolta, Carlo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3407128/ https://www.ncbi.nlm.nih.gov/pubmed/22848652 http://dx.doi.org/10.1371/journal.pone.0041902 |
Ejemplares similares
-
Mutational screening of splicing factor genes in cases with autosomal dominant retinitis pigmentosa
por: Benaglio, Paola, et al.
Publicado: (2014) -
CNOT3 Is a Modifier of PRPF31 Mutations in Retinitis Pigmentosa with Incomplete Penetrance
por: Venturini, Giulia, et al.
Publicado: (2012) -
Retinitis pigmentosa and allied conditions today: a paradigm of translational research
por: Ayuso, Carmen, et al.
Publicado: (2010) -
Whole Exome Analysis Identifies Frequent CNGA1 Mutations in Japanese Population with Autosomal Recessive Retinitis Pigmentosa
por: Katagiri, Satoshi, et al.
Publicado: (2014) -
Retinitis Pigmentosa: Genes and Disease Mechanisms
por: Ferrari, Stefano, et al.
Publicado: (2011)