DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions

MLA

Lidia Di Vito, et al. “DGUOK Recessive Mutations in Patients with CPEO, Mitochondrial Myopathy, Parkinsonism and MtDNA Deletions.” Brain, vol. 141, Dec. 2017, p. e3. 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.....05b76a0eec6fd8e7b04973c966467a2d&authtype=sso&custid=ns315887.

APA

Lidia Di Vito, Maria Lucia Valentino, Luca Bello, Francesca Tagliavini, Valerio Carelli, Chiara La Morgia, Leonardo Caporali, Rocco Liguori, Elena Pegoraro, Alessandra Maresca, & Diego Cecchin. (2017). DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions. Brain, 141, e3.

Chicago

Lidia Di Vito, Maria Lucia Valentino, Luca Bello, Francesca Tagliavini, Valerio Carelli, Chiara La Morgia, Leonardo Caporali, et al. 2017. “DGUOK Recessive Mutations in Patients with CPEO, Mitochondrial Myopathy, Parkinsonism and MtDNA Deletions.” Brain 141 (December): e3. 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.....05b76a0eec6fd8e7b04973c966467a2d&authtype=sso&custid=ns315887.