Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases

MLA

Ben Pode-Shakked, et al. “Exome Sequencing in Jewish and Arab Patients with Rhabdomyolysis Reveals Single-Gene Etiology in 43% of Cases.” Pediatric Nephrology, vol. 32, Aug. 2017, pp. 2273–82. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi.dedup.....8f5efd13b5eb588dd6c1f91a8eb699c5&authtype=sso&custid=ns315887.

APA

Ben Pode-Shakked, Adi Aran, Richard P. Lifton, Friedhelm Hildebrandt, Jing Chen, Omer Bar-Yosef, Shirlee Shril, Avraham Zeharia, Yair Anikster, Johanna Magdalena Schmidt, Yuval Landau, Reeval Segel, Nina Mann, Amelie T. van der Ven, Hadas Ityel, Annick Raas-Rothschild, Orna Staretz-Chacham, & Asaf Vivante. (2017). Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases. Pediatric Nephrology, 32, 2273–2282.

Chicago

Ben Pode-Shakked, Adi Aran, Richard P. Lifton, Friedhelm Hildebrandt, Jing Chen, Omer Bar-Yosef, Shirlee Shril, et al. 2017. “Exome Sequencing in Jewish and Arab Patients with Rhabdomyolysis Reveals Single-Gene Etiology in 43% of Cases.” Pediatric Nephrology 32 (August): 2273–82. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi.dedup.....8f5efd13b5eb588dd6c1f91a8eb699c5&authtype=sso&custid=ns315887.