Mutations in WDR4 as a new cause of Galloway-Mowat syndrome.

MLA

Braun, Daniela A., et al. “Mutations in WDR4 as a New Cause of Galloway-Mowat Syndrome.” American Journal of Medical Genetics. Part A, vol. 176, no. 11, Nov. 2018, pp. 2460–65. EBSCOhost, https://doi.org/10.1002/ajmg.a.40489.

APA

Braun, D. A., Shril, S., Sinha, A., Schneider, R., Tan, W., Ashraf, S., Hermle, T., Jobst-Schwan, T., Widmeier, E., Majmundar, A. J., Daga, A., Warejko, J. K., Nakayama, M., Schapiro, D., Chen, J., Airik, M., Rao, J., Schmidt, J. M., Hoogstraten, C. A., … Hildebrandt, F. (2018). Mutations in WDR4 as a new cause of Galloway-Mowat syndrome. American Journal of Medical Genetics. Part A, 176(11), 2460–2465. https://doi.org/10.1002/ajmg.a.40489

Chicago

Braun, Daniela A, Shirlee Shril, Aditi Sinha, Ronen Schneider, Weizhen Tan, Shazia Ashraf, Tobias Hermle, et al. 2018. “Mutations in WDR4 as a New Cause of Galloway-Mowat Syndrome.” American Journal of Medical Genetics. Part A 176 (11): 2460–65. doi:10.1002/ajmg.a.40489.