A novel missense mutation (H119L) identified in a Taiwan Chinese family with glycogen storage disease Ia (Von Gierke disease)

MLA

Mei-Chen Wu, et al. “A Novel Missense Mutation (H119L) Identified in a Taiwan Chinese Family with Glycogen Storage Disease Ia (Von Gierke Disease).” Human Mutation, vol. 16, Jan. 2000, p. 447. 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...........ff991a177d9485d1d16091c84e1049a8&authtype=sso&custid=ns315887.

APA

Mei-Chen Wu, Jer-Yuarn Wu, Fuu Jen Tsai, Cheng-Chun Lee, & Chang Hai Tsai. (2000). A novel missense mutation (H119L) identified in a Taiwan Chinese family with glycogen storage disease Ia (Von Gierke disease). Human Mutation, 16, 447.

Chicago

Mei-Chen Wu, Jer-Yuarn Wu, Fuu Jen Tsai, Cheng-Chun Lee, and Chang Hai Tsai. 2000. “A Novel Missense Mutation (H119L) Identified in a Taiwan Chinese Family with Glycogen Storage Disease Ia (Von Gierke Disease).” Human Mutation 16 (January): 447. 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...........ff991a177d9485d1d16091c84e1049a8&authtype=sso&custid=ns315887.