Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity

MLA

Braun, Daniela A., et al. Whole Exome Sequencing Identifies Causative Mutations in the Majority of Consanguineous or Familial Cases with Childhood-Onset Increased Renal Echogenicity. Jan. 2015. EBSCOhost, https://doi.org/10.1038/ki.2015.317.

APA

Braun, D. A., Schueler, M., Halbritter, J., Gee, H. Y., Porath, J. D., Lawson, J. A., Airik, R., Shril, S., Allen, S. J., Stein, D., Al Kindy, A., Beck, B. B., Cengiz, N., Moorani, K. N., Ozaltin, F., Hashmi, S., Sayer, J. A., Bockenhauer, D., Soliman, N. A., … Hildebrandt, F. (2015). Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity. https://doi.org/10.1038/ki.2015.317

Chicago

Braun, Daniela A., Markus Schueler, Jan Halbritter, Heon Yung Gee, Jonathan D. Porath, Jennifer A. Lawson, Rannar Airik, et al. 2015. “Whole Exome Sequencing Identifies Causative Mutations in the Majority of Consanguineous or Familial Cases with Childhood-Onset Increased Renal Echogenicity,” January. doi:10.1038/ki.2015.317.