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'
- PMID: 34611934
- DOI: 10.1111/evj.13503
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'
Comment on
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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 Nov;53(6):1296. doi: 10.1111/evj.13504. Equine Vet J. 2021. PMID: 34611935 No abstract available.
References
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- 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. https://doi.org/10.1111/evj.13504
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- Hack YL, Crabtree EE, Avila F, Sutton RB, Grahn R, Oh A, et al. 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.
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- Sandmeyer LS, Breaux CB, Archer S, Grahn BH. (2007), 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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