Whole‐genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse-Reference-Cited by-同舟云学术

Whole‐genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse

Published:2020-08-03 Issue:2 Volume:53 Page:316-323
ISSN:0425-1644
Container-title:Equine Veterinary Journal
language:en
Short-container-title:Equine Vet J

Author:

Hack Yael L.¹,Crabtree Elizabeth E.²,Avila Felipe¹,Sutton Roger B.³,Grahn Robert¹,Oh Annie²,Gilger Brian²,Bellone Rebecca R.¹⁴^ORCID

Affiliation:

1. Veterinary Genetics Laboratory School of Veterinary Medicine University of California Davis California USA

2. College of Veterinary Medicine North Carolina State University Raleigh North Carolina USA

3. Cell Physiology and Molecular Biophysics School of Medicine Texas Tech University Health Sciences Center Lubbock Texas USA

4. Population Health and Reproduction School of Veterinary Medicine University of California Davis California USA

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/evj.13318

Reference42 articles.

1. Congenital stationary night blindness in a Thoroughbred and a Paso Fino

2. Congenital stationary night blindness in the dog: common mutation in the RPE65 gene indicates founder effect;Aguirre GD;Mol Vision,1998

3. Molecular and immunohistochemical characterization of a canine model of complete congenital stationary night blindness (CSNB);Das G;Investig Ophthalmol Visual Sci,2014

4. Electroretinography in Cases of Night Blindness*

5. Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert–Bornschein type

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