Braun, D. A. Et Al. 2016. Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity. KIDNEY INTERNATIONAL , vol.89, no.2 , 468-475.

Braun, D. A., Schueler, M., Halbritter, J., Gee, H. Y., Porath, J. D., Lawson, J. A., ... Airik, R.(2016). Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity. KIDNEY INTERNATIONAL , vol.89, no.2, 468-475.

Braun, Daniela Et Al. "Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity," KIDNEY INTERNATIONAL , vol.89, no.2, 468-475, 2016

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." KIDNEY INTERNATIONAL , vol.89, no.2, pp.468-475, 2016

Braun, D. A. Et Al. (2016) . "Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity." KIDNEY INTERNATIONAL , vol.89, no.2, pp.468-475.

@article{article, author={Daniela A. Braun Et Al. }, title={Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity}, journal={KIDNEY INTERNATIONAL}, year=2016, pages={468-475} }