Cite
A novel splice variant in EMC1 is associated with cerebellar atrophy, visual impairment, psychomotor retardation with epilepsy
MLA
Lokesh Lingappa, et al. “A Novel Splice Variant in EMC1 Is Associated with Cerebellar Atrophy, Visual Impairment, Psychomotor Retardation with Epilepsy.” Molecular Genetics & Genomic Medicine, vol. 6, Dec. 2017, pp. 282–87. 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.....9b0313d4dab517d0061da37a8f2e5ef5&authtype=sso&custid=ns315887.
APA
Lokesh Lingappa, Hridya Govindan, Ramprasad Vedam, Ravi Gupta, Sakthivel Murugan, Thenral S. Geetha, Abhishek Ravindra Jain, & Nitin Mandloi. (2017). A novel splice variant in EMC1 is associated with cerebellar atrophy, visual impairment, psychomotor retardation with epilepsy. Molecular Genetics & Genomic Medicine, 6, 282–287.
Chicago
Lokesh Lingappa, Hridya Govindan, Ramprasad Vedam, Ravi Gupta, Sakthivel Murugan, Thenral S. Geetha, Abhishek Ravindra Jain, and Nitin Mandloi. 2017. “A Novel Splice Variant in EMC1 Is Associated with Cerebellar Atrophy, Visual Impairment, Psychomotor Retardation with Epilepsy.” Molecular Genetics & Genomic Medicine 6 (December): 282–87. 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.....9b0313d4dab517d0061da37a8f2e5ef5&authtype=sso&custid=ns315887.