Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population.

MLA

Polla, Daniel L., et al. “Phenotypic Spectrum Associated with a CRADD Founder Variant Underlying Frontotemporal Predominant Pachygyria in the Finnish Population.” European Journal of Human Genetics : EJHG, vol. 27, no. 8, Aug. 2019, pp. 1235–43. EBSCOhost, https://doi.org/10.1038/s41431-019-0383-8.

APA

Polla, D. L., Rahikkala, E., Bode, M. K., Määttä, T., Varilo, T., Loman, T., Philips, A. K., Kurki, M., Palotie, A., Körkkö, J., Vieira, P., Avela, K., Jacquemin, V., Pirson, I., Abramowicz, M., de Brouwer, A. P. M., Kuismin, O., van Bokhoven, H., & Järvelä, I. (2019). Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population. European Journal of Human Genetics : EJHG, 27(8), 1235–1243. https://doi.org/10.1038/s41431-019-0383-8

Chicago

Polla, Daniel L, Elisa Rahikkala, Michaela K Bode, Tuomo Määttä, Teppo Varilo, Thyrza Loman, Anju K Philips, et al. 2019. “Phenotypic Spectrum Associated with a CRADD Founder Variant Underlying Frontotemporal Predominant Pachygyria in the Finnish Population.” European Journal of Human Genetics : EJHG 27 (8): 1235–43. doi:10.1038/s41431-019-0383-8.