Subject
Genetics,Animal Science and Zoology,General Medicine
Reference86 articles.
1. Equine multiple congenital ocular anomalies maps to a 4.9 megabase interval on horse chromosome 6;Andersson;BMC Genetics,2008
2. TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness;Audo;American Journal of Human Genetics,2009
3. Analysis of a SNP in exon 7 of equine OCA2 and its exclusion as a cause for appaloosa spotting;Bellone;Animal Genetics,2006a
4. Comparative mapping of oculocutaneous albinism type II (OCA2), transient receptor potential cation channel, subfamily M member 1 (TRPM1) and two equine microsatellites, ASB08 and 1CA43, among four equid species by fluorescence in situ hybridization;Bellone;Cytogenetic and Genome Research,2006b
5. Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus);Bellone;Genetics,2008
Cited by
59 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献