Dominant PRPF31 Mutations Are Hypostatic to a Recessive CNOT3 Polymorphism in Retinitis Pigmentosa: A Novel Phenomenon of “Linked Trans-Acting Epistasis”

Mutations in PRPF31 are responsible for autosomal dominant retinitis pigmentosa (adRP, RP11 form) and affected families show nonpenetrance. Differential expression of the wildtype PRPF31 allele is responsible for this phenomenon: coinheritance of a mutation and a higher expressing wildtype allele pr...

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Detalles Bibliográficos
Autores principales: Rose, Anna M, Shah, Amna Z, Venturini, Giulia, Rivolta, Carlo, Rose, Geoffrey E, Bhattacharya, Shomi S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2013
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4240469/
https://www.ncbi.nlm.nih.gov/pubmed/24116917
http://dx.doi.org/10.1111/ahg.12042

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4240469/
https://www.ncbi.nlm.nih.gov/pubmed/24116917
http://dx.doi.org/10.1111/ahg.12042

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