APA (7th ed.) Citation

Hutter, S., Piro, R. M., Reuss, D., Hovestadt, V., Sahm, F., Farschtschi, S., . . . Mautner, V. F. (2014). Whole exome sequencing reveals that the majority of schwannomatosis cases remain unexplained after excluding SMARCB1 and LZTR1 germline variants. Acta neuropathologica, 128(3), . https://doi.org/10.1007/s00401-014-1311-1

Chicago Style (17th ed.) Citation

Hutter, Sonja, et al. "Whole Exome Sequencing Reveals That the Majority of Schwannomatosis Cases Remain Unexplained After Excluding SMARCB1 and LZTR1 Germline Variants." Acta Neuropathologica 128, no. 3 (2014). https://doi.org/10.1007/s00401-014-1311-1.

MLA (9th ed.) Citation

Hutter, Sonja, et al. "Whole Exome Sequencing Reveals That the Majority of Schwannomatosis Cases Remain Unexplained After Excluding SMARCB1 and LZTR1 Germline Variants." Acta Neuropathologica, vol. 128, no. 3, 2014, https://doi.org/10.1007/s00401-014-1311-1.