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.
No abstract available

Publication types

  • Letter
  • Comment

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

Supplementary concepts

  • Night blindness, congenital stationary