Redundant contribution of a Transient Receptor Potential cation channel Member 1 exon 11 single nucleotide polymorphism to equine congenital stationary night blindness

BACKGROUND: Congenital stationary night-blindness (CSNB) is a recessive autosomal defect in low-light vision in Appaloosa and other horse breeds. This condition has been mapped by linkage analysis to a gene coding for the Transient Receptor Potential cation channel Member 1 (TRPM1). TRPM1 is normall...

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Bibliografiset tiedot
Julkaisussa:BMC Vet Res
Päätekijät: Scott, Michelle L., John, Emily E., Bellone, Rebecca R., Ching, John C. H., Loewen, Matthew E., Sandmeyer, Lynne S., Grahn, Bruce H., Forsyth, George W.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2016
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4915136/
https://ncbi.nlm.nih.gov/pubmed/27329127
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12917-016-0745-1
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