APA (7th ed.) Citation

Salvoro, C., Bortoluzzi, S., Coppe, A., Valle, G., Feltrin, E., Mostacciuolo, M. L., & Vazza, G. (2018). Rare Risk Variants Identification by Identity-by-Descent Mapping and Whole-Exome Sequencing Implicates Neuronal Development Pathways in Schizophrenia and Bipolar Disorder. Molecular neurobiology, 55(9), 7366-7376. https://doi.org/10.1007/s12035-018-0922-2

Chicago Style (17th ed.) Citation

Salvoro, C., S. Bortoluzzi, A. Coppe, G. Valle, E. Feltrin, M. L. Mostacciuolo, and G. Vazza. "Rare Risk Variants Identification by Identity-by-Descent Mapping and Whole-Exome Sequencing Implicates Neuronal Development Pathways in Schizophrenia and Bipolar Disorder." Molecular Neurobiology 55, no. 9 (2018): 7366-7376. https://doi.org/10.1007/s12035-018-0922-2.

MLA (9th ed.) Citation

Salvoro, C., et al. "Rare Risk Variants Identification by Identity-by-Descent Mapping and Whole-Exome Sequencing Implicates Neuronal Development Pathways in Schizophrenia and Bipolar Disorder." Molecular Neurobiology, vol. 55, no. 9, 2018, pp. 7366-7376, https://doi.org/10.1007/s12035-018-0922-2.