论文信息 - Analysis of a SNP in exon 7 of equine OCA2 and its exclusion as a cause for appaloosa spotting. - 字舞流文

Analysis of a SNP in exon 7 of equine OCA2 and its exclusion as a cause for appaloosa spotting.

R. Bellone | S. Archer | E. Bailey | S. Lawson | N. Hunter

[1] D. Adelson,et al. 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 , 2006, Cytogenetic and Genome Research.

[2] S. Brooks,et al. Assignment of the appaloosa coat colour gene (LP) to equine chromosome 1. , 2004, Animal genetics.

[3] R. Spritz,et al. Frequent intragenic deletion of the P gene in Tanzanian patients with type II oculocutaneous albinism (OCA2). , 1995, American journal of human genetics.

[4] M. Lyon,et al. Genetic and molecular analysis of recessive alleles at the pink-eyed dilution (p) locus of the mouse. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[5] G. Carr,et al. The inheritance of the leopard complex of spotting patterns in horses. , 1990, The Journal of heredity.