Cite
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: phenotypical and genotypical characterization
MLA
Sergio Ferrari, et al. “A Novel Mutation of Aprataxin Associated with Ataxia Ocular Apraxia Type 1: Phenotypical and Genotypical Characterization.” Journal of the Neurological Sciences, vol. 260, no. 1–2, Jan. 2007. 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.....ad283b02179acbbcdea59d449e4b6083&authtype=sso&custid=ns315887.
APA
Sergio Ferrari, Nicolo’ Rizzuto, Gian Maria Fabrizi, Giovanna Squintani, Moreno Ferrarini, & Tiziana Cavallaro. (2007). A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: phenotypical and genotypical characterization. Journal of the Neurological Sciences, 260(1–2).
Chicago
Sergio Ferrari, Nicolo’ Rizzuto, Gian Maria Fabrizi, Giovanna Squintani, Moreno Ferrarini, and Tiziana Cavallaro. 2007. “A Novel Mutation of Aprataxin Associated with Ataxia Ocular Apraxia Type 1: Phenotypical and Genotypical Characterization.” Journal of the Neurological Sciences 260 (1–2). 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.....ad283b02179acbbcdea59d449e4b6083&authtype=sso&custid=ns315887.