A large deletion in RPGR causes XLPRA in Weimaraner dogs-Reference-Cited by-同舟云学术

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A large deletion in RPGR causes XLPRA in Weimaraner dogs

Published:2016-07-08 Issue:1 Volume:3 Page:
ISSN:2052-6687
Container-title:Canine Genetics and Epidemiology
language:en
Short-container-title:Canine Genet Epidemiol

Author:

Kropatsch Regina,Akkad Denis A.,Frank Matthias,Rosenhagen Carsten,Altmüller Janine,Nürnberg Peter,Epplen Jörg T.,Dekomien Gabriele

Publisher

Springer Science and Business Media LLC

Subject

General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s40575-016-0037-x

Reference31 articles.

1. Petersen-Jones S. Advances in the molecular understanding of canine retinal diseases. J Small Anim Pract. 2005;46:371–80.

2. Miyadera K, Acland GM, Aguirre GD. Genetic and phenotypic variations of inherited retinal diseases in dogs: the power of within- and across-breed studies. Mamm Genome. 2012;23:40–61.

3. Petersen-Jones SM, Komaromy AM. Dog models for blinding inherited retinal dystrophies. Hum Gene Ther Clin Dev. 2015;26:15–26.

4. Wiik AC, Ropstad EO, Ekesten B, Karlstam L, Wade CM, Lingaas F. Progressive retinal atrophy in Shetland sheepdog is associated with a mutation in the CNGA1 gene. Anim Genet. 2015;46:515–21.

5. Kijas JW, Cideciyan AV, Aleman TS, Pianta MJ, Pearce-kelling SE, Miller BJ, et al. Naturally occurring rhodopsin mutation in the dog causes retinal dysfunction and degeneration mimicking human dominant retinitis pigmentosa. Proc Natl Acad Sci U S A. 2002;99:6328–33.

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