APA (7th ed.) Citation

Brockmann, S. J., Freischmidt, A., Oeckl, P., Müller, K., Ponna, S. K., Helferich, A. M., . . . Weishaupt, J. H. (2018). CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency. Human molecular genetics, 27(4), . https://doi.org/10.1093/hmg/ddx436

Chicago Style (17th ed.) Citation

Brockmann, Sarah J., et al. "CHCHD10 Mutations P.R15L and P.G66V Cause Motoneuron Disease by Haploinsufficiency." Human Molecular Genetics 27, no. 4 (2018). https://doi.org/10.1093/hmg/ddx436.

MLA (9th ed.) Citation

Brockmann, Sarah J., et al. "CHCHD10 Mutations P.R15L and P.G66V Cause Motoneuron Disease by Haploinsufficiency." Human Molecular Genetics, vol. 27, no. 4, 2018, https://doi.org/10.1093/hmg/ddx436.