Cite
Early diagnosis of Pearson syndrome in neonatal intensive care following rapid mitochondrial genome sequencing in tandem with exome sequencing.
MLA
Stark Z., et al. Early Diagnosis of Pearson Syndrome in Neonatal Intensive Care Following Rapid Mitochondrial Genome Sequencing in Tandem with Exome Sequencing. 2019. 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=edsoai&AN=edsoai.on1305127279&authtype=sso&custid=ns315887.
APA
Stark Z., Akesson L.S., Eggers S., Love C.J., Chong B., Krzesinski E.I., Brown N.J., Tan T.Y., Richmond C.M., Thorburn D.R., Christodoulou J., Hunter M.F., & Lunke S. (2019). Early diagnosis of Pearson syndrome in neonatal intensive care following rapid mitochondrial genome sequencing in tandem with exome sequencing.
Chicago
Stark Z., Akesson L.S., Eggers S., Love C.J., Chong B., Krzesinski E.I., Brown N.J., et al. 2019. “Early Diagnosis of Pearson Syndrome in Neonatal Intensive Care Following Rapid Mitochondrial Genome Sequencing in Tandem with Exome Sequencing.” 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=edsoai&AN=edsoai.on1305127279&authtype=sso&custid=ns315887.