HMG CoA lyase deficiency: identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41Q

MLA

Mitchell, Grant A., et al. “HMG CoA Lyase Deficiency: Identification of Five Causal Point Mutations in Codons 41 and 42, Including a Frequent Saudi Arabian Mutation, R41Q.” American Journal of Human Genetics, vol. 62, no. 2, Feb. 1998, p. 295. 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.53712163&authtype=sso&custid=ns315887.

APA

Mitchell, G. A., Ozand, P. T., Robert, M. F., Ashmarina, L., Roberts, J., Gibson, K. M., Wanders, R. J., Wang, S., Chevalier, I., Plochl, E., & Miziorko, H. (1998). HMG CoA lyase deficiency: identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41Q. American Journal of Human Genetics, 62(2), 295.

Chicago

Mitchell, Grant A., Pinar T. Ozand, Marie, France Robert, Lyudmila Ashmarina, Jacqueline Roberts, K. Michael Gibson, Ronald J. Wanders, et al. 1998. “HMG CoA Lyase Deficiency: Identification of Five Causal Point Mutations in Codons 41 and 42, Including a Frequent Saudi Arabian Mutation, R41Q.” American Journal of Human Genetics 62 (2): 295. 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.53712163&authtype=sso&custid=ns315887.