Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses.

MLA

Bellone, Rebecca R., et al. “Fine-Mapping and Mutation Analysis of TRPM1: A Candidate Gene for Leopard Complex (LP) Spotting and Congenital Stationary Night Blindness in Horses.” Briefings in Functional Genomics, vol. 9, no. 3, May 2010, pp. 193–207. EBSCOhost, https://doi.org/10.1093/bfgp/elq002.

APA

Bellone, R. R., Forsyth, G., Leeb, T., Archer, S., Sigurdsson, S., Imsland, F., Mauceli, E., Engensteiner, M., Bailey, E., Sandmeyer, L., Grahn, B., Lindblad-Toh, K., & Wade, C. M. (2010). Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses. Briefings in Functional Genomics, 9(3), 193–207. https://doi.org/10.1093/bfgp/elq002

Chicago

Bellone, Rebecca R, George Forsyth, Tosso Leeb, Sheila Archer, Snaevar Sigurdsson, Freyja Imsland, Evan Mauceli, et al. 2010. “Fine-Mapping and Mutation Analysis of TRPM1: A Candidate Gene for Leopard Complex (LP) Spotting and Congenital Stationary Night Blindness in Horses.” Briefings in Functional Genomics 9 (3): 193–207. doi:10.1093/bfgp/elq002.