Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding NPHP1 deletions.

MLA

Deutsch, Konstantin, et al. “Exome Sequencing Identifies a Likely Causative Variant in 53% of Families with Ciliopathy-Related Features on Renal Ultrasound after Excluding NPHP1 Deletions.” Genes & Diseases, vol. 11, no. 5, Sept. 2023, p. 101111. EBSCOhost, https://doi.org/10.1016/j.gendis.2023.101111.

APA

Deutsch, K., Klämbt, V., Kitzler, T. M., Jobst-Schwan, T., Schneider, R., Buerger, F., Seltzsam, S., El Desoky, S., Kari, J. A., Hafeez, F., Szczepańska, M., Eid, L. A., Awad, H. S., Al-Saffar, M., Soliman, N. A., Tasic, V., Nicolas-Frank, C., Yousef, K., Schierbaum, L. M., … Hildebrandt, F. (2023). Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding NPHP1 deletions. Genes & Diseases, 11(5), 101111. https://doi.org/10.1016/j.gendis.2023.101111

Chicago

Deutsch, Konstantin, Verena Klämbt, Thomas M Kitzler, Tilman Jobst-Schwan, Ronen Schneider, Florian Buerger, Steve Seltzsam, et al. 2023. “Exome Sequencing Identifies a Likely Causative Variant in 53% of Families with Ciliopathy-Related Features on Renal Ultrasound after Excluding NPHP1 Deletions.” Genes & Diseases 11 (5): 101111. doi:10.1016/j.gendis.2023.101111.