Vivante, A., Ityel, H., Pode-Shakked, B., Chen, J., Shril, S., van der Ven, A. T., . . . Hildebrandt, F. (2017). Exome sequencing in Jewish and Arabic patients with rhabdomyolysis reveals single-gene etiology in 43% of cases. Pediatr Nephrol.

Vivante, Asaf, et al. "Exome Sequencing in Jewish and Arabic Patients With Rhabdomyolysis Reveals Single-gene Etiology in 43% of Cases." Pediatr Nephrol 2017.

Vivante, Asaf, et al. "Exome Sequencing in Jewish and Arabic Patients With Rhabdomyolysis Reveals Single-gene Etiology in 43% of Cases." Pediatr Nephrol 2017.