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: 34611935
- DOI: 10.1111/evj.13504
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 in
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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. 2021 Nov;53(6):1297. doi: 10.1111/evj.13503. Equine Vet J. 2021. PMID: 34611934 No abstract available.
Comment on
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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 Mar;53(2):316-323. doi: 10.1111/evj.13318. Epub 2020 Aug 3. Equine Vet J. 2021. PMID: 32654228
References
REFERENCES
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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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- Corboy JM. A review of optics. In: Corboy JM, editor. The Retinoscopy Book. Thorofare: SLACK Incorporated, 2003; p. 17-23.
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- Bracun A, Ellis AD, Hall C. A retinoscopic survey of 333 horses and ponies in the UK. Vet Ophthalmol. 2014;17(Suppl 1):90-6.
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