Cerny, D., Thi Le, D., The, T., Zuest, R., Kg, S., Velumani, S., . . . Fink, K. (2016). Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence. Elsevier.
Chicago Style (17th ed.) CitationCerny, D., et al. Complete Human CD1a Deficiency on Langerhans Cells Due to a Rare Point Mutation in the Coding Sequence. Elsevier, 2016.
MLA引文Cerny, D., et al. Complete Human CD1a Deficiency on Langerhans Cells Due to a Rare Point Mutation in the Coding Sequence. Elsevier, 2016.
警告：這些引文格式不一定是100％准確.