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Comment
. 2021 Nov;53(6):1297.
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'

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Comment

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'

Brian Gilger et al. Equine Vet J. 2021 Nov.
No abstract available

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Comment on

References

    1. 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
    1. 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.
    1. 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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