APA (7th ed.) Citation

M, B., SP, A., A, N., E, H., M, B., SP, T., . . . P, K. (2020). Mutations in GRK2 cause Jeune syndrome by impairing Hedgehog and canonical Wnt signaling. EMBO molecular medicine, 12(11), e11739. https://doi.org/10.15252/emmm.201911739

Chicago Style (17th ed.) Citation

M, Bosakova, et al. "Mutations in GRK2 Cause Jeune Syndrome by Impairing Hedgehog and Canonical Wnt Signaling." EMBO Molecular Medicine 12, no. 11 (2020): e11739. https://doi.org/10.15252/emmm.201911739.

MLA (9th ed.) Citation

M, Bosakova, et al. "Mutations in GRK2 Cause Jeune Syndrome by Impairing Hedgehog and Canonical Wnt Signaling." EMBO Molecular Medicine, vol. 12, no. 11, 2020, p. e11739, https://doi.org/10.15252/emmm.201911739.