ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme [Q.sub.10] deficiency

MLA

Lagier-Tourenne, Clotilde, et al. “ADCK3, an Ancestral Kinase, Is Mutated in a Form of Recessive Ataxia Associated with Coenzyme [Q.Sub.10] Deficiency.” American Journal of Human Genetics, vol. 82, no. 3, Mar. 2008, p. 661. 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=edsggo&AN=edsgcl.177044273&authtype=sso&custid=ns315887.

APA

Lagier-Tourenne, C., Tazir, M., Lopez, L. C., Quinzii, C. M., Assoum, M., Drouot, N., Koenig, M., Busso, C., Makri, S., Ali-Pacha, L., Benhassine, T., Hirano, M., Anheim, M., Lynch, D. R., Thibault, C., Plewniak, F., Bianchetti, L., Tranchant, C., Poch, O., … Barros, M. H. (2008). ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme [Q.sub.10] deficiency. American Journal of Human Genetics, 82(3), 661.

Chicago

Lagier-Tourenne, Clotilde, Meriem Tazir, Luis Carlos Lopez, Catarina M. Quinzii, Mirna Assoum, Nathalie Drouot, Michel Koenig, et al. 2008. “ADCK3, an Ancestral Kinase, Is Mutated in a Form of Recessive Ataxia Associated with Coenzyme [Q.Sub.10] Deficiency.” American Journal of Human Genetics 82 (3): 661. 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=edsggo&AN=edsgcl.177044273&authtype=sso&custid=ns315887.