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Maaser, A., Strohmaier, J., Ludwig, K. U., Degenhardt, F., Streit, F., Schenk, L. M., Koller, A. C., Fischer, S. B., Thiele, H., Nuernberg, P., Guzman-Parra, J., Orozco Diaz, G., Auburger, G., Albus, M., Borrmann-Hassenbach, M., Jose Gonzalez, M., Gil Flores, S., Cabaleiro Fabeiro, F. J., del Rio Noriega, F., Perez Perez, F., Haro Gonzalez, J., Rivas, F., Mayoral, F., Herms, S., Hoffmann, P., Cichon, S., Rietschel, M., Noethen, M. M. and Forstner, A. J. (2018). Exome sequencing of multiply affected bipolar disorder families and follow-up resequencing implicate rare variants in neuronal genes contributing to disease etiology. Eur. J. Hum. Genet., 26. S. 373 - 375. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5438

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