CA8 mutations cause a novel syndrome characterized by ataxia and mild mental retardation with predisposition to quadrupedal gait.

MLA

Türkmen, Seval, et al. “CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait.” PLoS Genetics, vol. 5, no. 5, May 2009, p. e1000487. EBSCOhost, https://doi.org/10.1371/journal.pgen.1000487.

APA

Türkmen, S., Guo, G., Garshasbi, M., Hoffmann, K., Alshalah, A. J., Mischung, C., Kuss, A., Humphrey, N., Mundlos, S., & Robinson, P. N. (2009). CA8 mutations cause a novel syndrome characterized by ataxia and mild mental retardation with predisposition to quadrupedal gait. PLoS Genetics, 5(5), e1000487. https://doi.org/10.1371/journal.pgen.1000487

Chicago

Türkmen, Seval, Gao Guo, Masoud Garshasbi, Katrin Hoffmann, Amjad J Alshalah, Claudia Mischung, Andreas Kuss, Nicholas Humphrey, Stefan Mundlos, and Peter N Robinson. 2009. “CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait.” PLoS Genetics 5 (5): e1000487. doi:10.1371/journal.pgen.1000487.