APA (7th ed.) Citation

Jackson, C., Bauer, M., Schaller, A., Kotzaeridou, U., Ferrarini, A., Hahn, D., . . . Bonafé, L. (2016). A novel mutation in BCS1L associated with deafness, tubulopathy, growth retardation and microcephaly. European Journal of Pediatrics, 175(4), 517. https://doi.org/10.1007/s00431-015-2661-y

Chicago Style (17th ed.) Citation

Jackson, C., et al. "A Novel Mutation in BCS1L Associated with Deafness, Tubulopathy, Growth Retardation and Microcephaly." European Journal of Pediatrics 175, no. 4 (2016): 517. https://doi.org/10.1007/s00431-015-2661-y.

MLA (9th ed.) Citation

Jackson, C., et al. "A Novel Mutation in BCS1L Associated with Deafness, Tubulopathy, Growth Retardation and Microcephaly." European Journal of Pediatrics, vol. 175, no. 4, 2016, p. 517, https://doi.org/10.1007/s00431-015-2661-y.