EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations.

MLA

Eggens, Veerle Rc, et al. “EXOSC3 Mutations in Pontocerebellar Hypoplasia Type 1: Novel Mutations and Genotype-Phenotype Correlations.” Orphanet Journal of Rare Diseases, vol. 9, Feb. 2014, p. 23. EBSCOhost, https://doi.org/10.1186/1750-1172-9-23.

APA

Eggens, V. R., Barth, P. G., Niermeijer, J.-M. F., Berg, J. N., Darin, N., Dixit, A., Fluss, J., Foulds, N., Fowler, D., Hortobágyi, T., Jacques, T., King, M. D., Makrythanasis, P., Máté, A., Nicoll, J. A. R., O’Rourke, D., Price, S., Williams, A. N., Wilson, L., … Baas, F. (2014). EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations. Orphanet Journal of Rare Diseases, 9, 23. https://doi.org/10.1186/1750-1172-9-23

Chicago

Eggens, Veerle Rc, Peter G Barth, Jikke-Mien F Niermeijer, Jonathan N Berg, Niklas Darin, Abhijit Dixit, Joel Fluss, et al. 2014. “EXOSC3 Mutations in Pontocerebellar Hypoplasia Type 1: Novel Mutations and Genotype-Phenotype Correlations.” Orphanet Journal of Rare Diseases 9 (February): 23. doi:10.1186/1750-1172-9-23.