Identification and functional characterization of a novel homozygous mutation in KCNMA1 encoding voltage and calcium sensitive potassium channel is associated with dyskinesia, epilepsy, intellectual disability, cerebellar and corticospinal tract atrophy

MLA

Yücesan, Emrah, et al. Identification and Functional Characterization of a Novel Homozygous Mutation in KCNMA1 Encoding Voltage and Calcium Sensitive Potassium Channel Is Associated with Dyskinesia, Epilepsy, Intellectual Disability, Cerebellar and Corticospinal Tract Atrophy. Jan. 2020. 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.dedup.wf.001..1cf1a8535ea10ca3fb6021710116af6c&authtype=sso&custid=ns315887.

APA

Yücesan, E., Goncu, B., Aslanger, A., Ozgul, C., Hasanoglu, S., & Yesil, G. (2020). Identification and functional characterization of a novel homozygous mutation in KCNMA1 encoding voltage and calcium sensitive potassium channel is associated with dyskinesia, epilepsy, intellectual disability, cerebellar and corticospinal tract atrophy.

Chicago

Yücesan, Emrah, Beyza Goncu, A. Aslanger, C. Ozgul, S. Hasanoglu, and G. Yesil. 2020. “Identification and Functional Characterization of a Novel Homozygous Mutation in KCNMA1 Encoding Voltage and Calcium Sensitive Potassium Channel Is Associated with Dyskinesia, Epilepsy, Intellectual Disability, Cerebellar and Corticospinal Tract Atrophy,” January. 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.dedup.wf.001..1cf1a8535ea10ca3fb6021710116af6c&authtype=sso&custid=ns315887.