D. Phillip Sponenberg: The inheritance of leopard spotting in the Noriker horse. In: The Journal of Heredity. 5. Jahrgang, Nr.73. The American Genetic Association, 1982, S.357–359, doi:10.1093/oxfordjournals.jhered.a109669 (englisch).
Rebecca R. Bellone, Heather Holl, Vijayasaradhi Setaluri, Sulochana Devi, Nityanand Maddodi, Sheila Archer, Lynne Sandmeyer, Arne Ludwig, Daniel Foerster, Melanie Pruvost, Monika Reissmann, Ralf Bortfeldt, David L. Adelson, Sim Lin Lim, Janelle Nelson, Bianca Haase, Martina Engensteiner, Tosso Leeb, George Forsyth, Michael J. Mienaltowski, Padmanabhan Mahadevan, Michael Hofreiter, Johanna L. A. Paijmans, Gloria Gonzalez-Fortes, Bruce Grahn, Samantha A. Brooks: Evidence for a Retroviral Insertion in TRPM1 as the Cause of Congenital Stationary Night Blindness and Leopard Complex Spotting in the Horse. In: PLOS ONE. 8. Jahrgang, Nr.10, 2013, S.e78280, doi:10.1371/journal.pone.0078280, PMID 24167615, PMC 3805535 (freier Volltext) – (englisch).
R. B. Terry, E. Bailey, T. Lear, E. G. Cothran: Rejection of MITF and MGF as the genes responsible for appaloosa coat colour patterns in horses. In: Animal Genetics. Band33, Nr.1, 2002, S.82–84, doi:10.1046/j.1365-2052.2002.0742h.x.
R. B. Terry, S. Archer, S. Brooks, D. Bernoco, E. Bailey: Assignment of the appaloosa coat colour gene (LP) to equine chromosome 1. In: Animal Genetics. Band35, Nr.2, 2004, S.134–137, doi:10.1111/j.1365-2052.2004.01113.x.
Lynne S. Sandmeyer, Breaux CB, Archer S, Grahn BH: Clinical and electroretinographic characteristics of congenital stationary night blindness in the Appaloosa and the association with the leopard complex. In: Veterinary Ophthalmology. 6. Jahrgang, Nr.10, 2007, S.368–375, doi:10.1111/j.1463-5224.2007.00572.x, PMID 17970998 (englisch).
Rebecca R Bellone, Brooks SA, Sandmeyer L, Murphy BA, Forsyth G, Archer S, Bailey E, Grahn B: Differential Gene Expression of TRPM1, the Potential Cause of Congenital Stationary Night Blindness and Coat Spotting Patterns (LP) in the Appaloosa Horse (Equus caballus). In: Genetics. 179. Jahrgang, Nr.4. Genetics Society of America, August 2008, S.1861–1870, doi:10.1534/genetics.108.088807, PMID 18660533, PMC 2516064 (freier Volltext) – (englisch).
D. P. Sponenberg, G. Carr, E. Simak, K. D. P. Schwink: The inheritance of the leopard complex of spotting patterns in horses. In: Journal of Heredity. Band81, Nr.4, 1990, S.323–331, PMID 2177073.
Rebecca R. Bellone, Heather Holl, Vijayasaradhi Setaluri, Sulochana Devi, Nityanand Maddodi, Sheila Archer, Lynne Sandmeyer, Arne Ludwig, Daniel Foerster, Melanie Pruvost, Monika Reissmann, Ralf Bortfeldt, David L. Adelson, Sim Lin Lim, Janelle Nelson, Bianca Haase, Martina Engensteiner, Tosso Leeb, George Forsyth, Michael J. Mienaltowski, Padmanabhan Mahadevan, Michael Hofreiter, Johanna L. A. Paijmans, Gloria Gonzalez-Fortes, Bruce Grahn, Samantha A. Brooks: Evidence for a Retroviral Insertion in TRPM1 as the Cause of Congenital Stationary Night Blindness and Leopard Complex Spotting in the Horse. In: PLOS ONE. 8. Jahrgang, Nr.10, 2013, S.e78280, doi:10.1371/journal.pone.0078280, PMID 24167615, PMC 3805535 (freier Volltext) – (englisch).
R. R. Terry, E. Bailey, D. Bernoco, E. G. Cothran: Linked markers exclude KIT as the gene responsible for appaloosa coat colour spotting patterns in horses. In: Animal Genetics. Band32, Nr.2, 2001, S.98–101, PMID 11421946.
R. Bellone, S. Lawson, N. Hunter, S. Archer, E. Bailey: Analysis of a SNP in exon 7 of equine OCA2 and its exclusion as a cause for appaloosa spotting. In: Animal Genetics. Band37, Nr.5, 2006, S.525, PMID 16978190.
R. R. Bellone, S. A. Brooks, L. Sandmeyer, B. A. Murphy, G. Forsyth, S. Archer, E. Bailey, B. Grahn: Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus). In: Animal Genetics. Band179, Nr.4, 2008, S.1861–1870, PMID 18660533.
L. S. Sandmeyer, C. B. Breaux, S. Archer, B. H. Grahn: Clinical and electroretinographic characteristics of congenital stationary night blindness in the Appaloosa and the association with the leopard complex. In: Veterinary Ophthalmology. Band10, Nr.6, 2007, S.368–375, PMID 17970998.
Lynne S. Sandmeyer, Breaux CB, Archer S, Grahn BH: Clinical and electroretinographic characteristics of congenital stationary night blindness in the Appaloosa and the association with the leopard complex. In: Veterinary Ophthalmology. 6. Jahrgang, Nr.10, 2007, S.368–375, doi:10.1111/j.1463-5224.2007.00572.x, PMID 17970998 (englisch).
Rebecca R Bellone, Brooks SA, Sandmeyer L, Murphy BA, Forsyth G, Archer S, Bailey E, Grahn B: Differential Gene Expression of TRPM1, the Potential Cause of Congenital Stationary Night Blindness and Coat Spotting Patterns (LP) in the Appaloosa Horse (Equus caballus). In: Genetics. 179. Jahrgang, Nr.4. Genetics Society of America, August 2008, S.1861–1870, doi:10.1534/genetics.108.088807, PMID 18660533, PMC 2516064 (freier Volltext) – (englisch).
M. Pruvost, R. Bellone, N. Benecke, E. Sandoval-Castellanos, M. Cieslak, T. Kuznetsova, A. Morales-Muñiz, T. O’Connor, M. Reissmann, M. Hofreiter, A. Ludwig: Genotypes of predomestic horses match phenotypes painted in Paleolithic works of cave art. In: Proc Natl Acad Sci U S A. 108(46), 15. Nov 2011, S. 18626–18630. Epub 2011 Nov 7. PMID 22065780
Sandmeyer, Lynne: Equine Recurrent Uveitis (ERU). The Appaloosa Project, 28. Juli 2008, archiviert vom Original am 26. April 2009; abgerufen am 21. März 2010 (englisch).
History of the Appaloosa. In: Appaloosa Museum. Archiviert vom Original (nicht mehr online verfügbar) am 18. Januar 2008; abgerufen am 1. Juni 2011.
Sandmeyer, Lynne: Equine Recurrent Uveitis (ERU). The Appaloosa Project, 28. Juli 2008, archiviert vom Original am 26. April 2009; abgerufen am 21. März 2010 (englisch).
History of the Appaloosa. In: Appaloosa Museum. Archiviert vom Original (nicht mehr online verfügbar) am 18. Januar 2008; abgerufen am 1. Juni 2011.
