APA (7th ed.) Citation

Assmann, G., Köhm, M., Schuster, V., Behrens, F., Mössner, R., Magnolo, N., . . . Hüffmeier, U. (2020). Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups. BMC Medical Genetics, 21(1), 1. https://doi.org/10.1186/s12881-020-01037-7

Chicago Style (17th ed.) Citation

Assmann, Gunter, Michaela Köhm, Volker Schuster, Frank Behrens, Rotraut Mössner, Nina Magnolo, Vinzenz Oji, Harald Burkhardt, and Ulrike Hüffmeier. "Genetic Variants in FBLIM1 Gene Do Not Contribute to SAPHO Syndrome and Chronic Recurrent Multifocal Osteomyelitis in Typical Patient Groups." BMC Medical Genetics 21, no. 1 (2020): 1. https://doi.org/10.1186/s12881-020-01037-7.

MLA (9th ed.) Citation

Assmann, Gunter, et al. "Genetic Variants in FBLIM1 Gene Do Not Contribute to SAPHO Syndrome and Chronic Recurrent Multifocal Osteomyelitis in Typical Patient Groups." BMC Medical Genetics, vol. 21, no. 1, 2020, p. 1, https://doi.org/10.1186/s12881-020-01037-7.