Deleterious variants in CRLS1 lead to cardiolipin deficiency and cause an autosomal recessive multi-system mitochondrial disease

MLA

Lee, Rg, et al. Deleterious Variants in CRLS1 Lead to Cardiolipin Deficiency and Cause an Autosomal Recessive Multi-System Mitochondrial Disease. 2022. 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.on1397537902&authtype=sso&custid=ns315887.

APA

Lee, R., Balasubramaniam, S., Stentenbach, M., Kralj, T., McCubbin, T., Padman, B., Smith, J., Riley, L., Priyadarshi, A., Peng, L., Nuske, M., Webster, R., Peacock, K., Roberts, P., Stark, Z., Lemire, G., Ito, Y., Boycott, K., Geraghty, M., … Filipovska, A. (2022). Deleterious variants in CRLS1 lead to cardiolipin deficiency and cause an autosomal recessive multi-system mitochondrial disease.

Chicago

Lee, Rg, S Balasubramaniam, M Stentenbach, T Kralj, T McCubbin, B Padman, J Smith, et al. 2022. “Deleterious Variants in CRLS1 Lead to Cardiolipin Deficiency and Cause an Autosomal Recessive Multi-System Mitochondrial Disease.” 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.on1397537902&authtype=sso&custid=ns315887.