Cite
ASAH1 variant causing a mild SMA phenotype with no myoclonic epilepsy: a clinical, biochemical and molecular study
MLA
Viviana Pensato, et al. ASAH1 Variant Causing a Mild SMA Phenotype with No Myoclonic Epilepsy: A Clinical, Biochemical and Molecular Study. Mar. 2016. 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.....f2136782f46013b884234442054c66c8&authtype=sso&custid=ns315887.
APA
Viviana Pensato, Mirella Filocamo, Massimiliano Filosto, Alessandro Padovani, Manuela Valsecchi, Fabrizio Rinaldi, Domitilla Schiumarini, Silvia Rota, Susanna Lualdi, Massimo Aureli, Raffaella Mazzotti, Barbara Castellotti, & Cinzia Gellera. (2016). ASAH1 variant causing a mild SMA phenotype with no myoclonic epilepsy: a clinical, biochemical and molecular study.
Chicago
Viviana Pensato, Mirella Filocamo, Massimiliano Filosto, Alessandro Padovani, Manuela Valsecchi, Fabrizio Rinaldi, Domitilla Schiumarini, et al. 2016. “ASAH1 Variant Causing a Mild SMA Phenotype with No Myoclonic Epilepsy: A Clinical, Biochemical and Molecular Study,” March. 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.....f2136782f46013b884234442054c66c8&authtype=sso&custid=ns315887.