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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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4915136/
https://www.ncbi.nlm.nih.gov/pubmed/27329127
http://dx.doi.org/10.1186/s12917-016-0745-1

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