Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase gene

MLA

Pirulli, D., et al. “Molecular Analysis of Hyperoxaluria Type 1 in Italian Patients Reveals Eight New Mutations in the Alanine: Glyoxylate Aminotransferase Gene.” Human Genetics, vol. 104, no. 6, Aug. 1999. 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.....d70f3d0f10dc3b97adeb7d1acf9874c4&authtype=sso&custid=ns315887.

APA

Pirulli, D., Puzzer, D., Ferretini, C., Ferri, L., Crovella, S., Amoroso, A., Marangella, M., Mazzola, G., & Florian, F. (1999). Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase gene. Human Genetics, 104(6).

Chicago

Pirulli, D, D Puzzer, C Ferretini, L Ferri, Sergio Crovella, A Amoroso, M Marangella, G Mazzola, and Fiorella Florian. 1999. “Molecular Analysis of Hyperoxaluria Type 1 in Italian Patients Reveals Eight New Mutations in the Alanine: Glyoxylate Aminotransferase Gene.” Human Genetics 104 (6). 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.....d70f3d0f10dc3b97adeb7d1acf9874c4&authtype=sso&custid=ns315887.