Response to comments on ‘Whole-genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse’.
Abstract: No abstract available
Publication Date: 2021-10-07 PubMed ID: 34611934DOI: 10.1111/evj.13503Google Scholar: Lookup
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Cite This Article
APA
Gilger B, Bellone RR.
(2021).
Response to comments on ‘Whole-genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse’.
Equine Vet J, 53(6), 1297.
https://doi.org/10.1111/evj.13503 Publication
Researcher Affiliations
- College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina, USA.
- Veterinary Genetics Laboratory, School of Veterinary Medicine, University of California, Davis, California, USA.
- Population Health and Reproduction, School of Veterinary Medicine, University of California, Davis, California, USA.
MeSH Terms
- Animals
- Eye Diseases, Hereditary / veterinary
- Genetic Diseases, X-Linked
- Horse Diseases / genetics
- Horses
- Mutation, Missense
- Myopia
- Night Blindness / genetics
- Night Blindness / veterinary
- Tennessee
References
This article includes 3 references
- McMullen RJ. Comments on ‘Whole-genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse’. Equine Vet J 2021;53:1296.
- Hack YL, Crabtree EE, Avila F, Sutton RB, Grahn R, Oh A. Whole-genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse. Equine Vet J 2021;53:316-23.
- Sandmeyer LS, Breaux CB, Archer S, Grahn BH. Clinical and electroretinographic characteristics of congenital stationary night blindness in the Appaloosa and the association with the leopard complex. Vet Ophthalmol 2007;10:368-75.
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