APA citiranje

Shamseldin, H., Faqeih, E., Alasmari, A., Zaki, M., Gleeson, J., & Alkuraya, F. (2016). Mutations in UNC80, Encoding Part of the UNC79-UNC80-NALCN Channel Complex, Cause Autosomal-Recessive Severe Infantile Encephalopathy. Am J Hum Genet.

Citação norma Chicago

Shamseldin, Hanan E., Eissa Faqeih, Ali Alasmari, Maha S Zaki, Joseph G Gleeson, and Fowzan S Alkuraya. "Mutations in UNC80, Encoding Part of the UNC79-UNC80-NALCN Channel Complex, Cause Autosomal-Recessive Severe Infantile Encephalopathy." Am J Hum Genet 2016.

MLA citiranje

Shamseldin, Hanan E., et al. "Mutations in UNC80, Encoding Part of the UNC79-UNC80-NALCN Channel Complex, Cause Autosomal-Recessive Severe Infantile Encephalopathy." Am J Hum Genet 2016.