APA (7th ed.) Citation

Hayer, S. N., Deconinck, T., Bender, B., Smets, K., Züchner, S., Reich, S., . . . Synofzik, M. (2017). STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: Evidence from four novel mutations. Orphanet journal of rare diseases, 12(1), 31. https://doi.org/10.1186/s13023-017-0580-x

Chicago Style (17th ed.) Citation

Hayer, Stefanie Nicole, et al. "STUB1/CHIP Mutations Cause Gordon Holmes Syndrome as Part of a Widespread Multisystemic Neurodegeneration: Evidence from Four Novel Mutations." Orphanet Journal of Rare Diseases 12, no. 1 (2017): 31. https://doi.org/10.1186/s13023-017-0580-x.

MLA (9th ed.) Citation

Hayer, Stefanie Nicole, et al. "STUB1/CHIP Mutations Cause Gordon Holmes Syndrome as Part of a Widespread Multisystemic Neurodegeneration: Evidence from Four Novel Mutations." Orphanet Journal of Rare Diseases, vol. 12, no. 1, 2017, p. 31, https://doi.org/10.1186/s13023-017-0580-x.