Cite
Genome-wide mRNA sequencing of a single canine cerebellar cortical degeneration case leads to the identification of a disease associated SPTBN2 mutation.
MLA
Forman, Oliver P., et al. “Genome-Wide MRNA Sequencing of a Single Canine Cerebellar Cortical Degeneration Case Leads to the Identification of a Disease Associated SPTBN2 Mutation.” BMC Genetics, vol. 13, no. 1, Jan. 2012, pp. 55–65. EBSCOhost, https://doi.org/10.1186/1471-2156-13-55.
APA
Forman, O. P., De Risio, L., Stewart, J., Mellersh, C. S., & Beltran, E. (2012). Genome-wide mRNA sequencing of a single canine cerebellar cortical degeneration case leads to the identification of a disease associated SPTBN2 mutation. BMC Genetics, 13(1), 55–65. https://doi.org/10.1186/1471-2156-13-55
Chicago
Forman, Oliver P., Luisa De Risio, Jennifer Stewart, Cathryn S. Mellersh, and Elsa Beltran. 2012. “Genome-Wide MRNA Sequencing of a Single Canine Cerebellar Cortical Degeneration Case Leads to the Identification of a Disease Associated SPTBN2 Mutation.” BMC Genetics 13 (1): 55–65. doi:10.1186/1471-2156-13-55.