APA citiranje

Wong, S., Lu, C. P., & Roth, D. B. (2008). A RAG1 mutation found in Omenn Syndrome causes coding flank hypersensitivity: A novel mechanism for antigen receptor repertoire restriction.

Citação norma Chicago

Wong, Serre-Yu, Catherine P. Lu, and David B. Roth. A RAG1 Mutation Found in Omenn Syndrome Causes Coding Flank Hypersensitivity: A Novel Mechanism for Antigen Receptor Repertoire Restriction. 2008.

MLA citiranje

Wong, Serre-Yu, Catherine P. Lu, and David B. Roth. A RAG1 Mutation Found in Omenn Syndrome Causes Coding Flank Hypersensitivity: A Novel Mechanism for Antigen Receptor Repertoire Restriction. 2008.