APA (7th ed.) Citation

Liao, C., Yu, H., Cheng, C., Chen, J., Lin, C., Chen, P., & Shieh, C. (2020). A novel pathogenic mutation on Interleukin-7 receptor leading to severe combined immunodeficiency identified with newborn screening and whole exome sequencing. Elsevier.

Chicago Style (17th ed.) Citation

Liao, Cheng-Yu, Hui-Wen Yu, Chao-Neng Cheng, Jiann-Shiuh Chen, Ching-Wei Lin, Peng-Chieh Chen, and Chi-Chang Shieh. A Novel Pathogenic Mutation on Interleukin-7 Receptor Leading to Severe Combined Immunodeficiency Identified with Newborn Screening and Whole Exome Sequencing. Elsevier, 2020.

MLA (9th ed.) Citation

Liao, Cheng-Yu, et al. A Novel Pathogenic Mutation on Interleukin-7 Receptor Leading to Severe Combined Immunodeficiency Identified with Newborn Screening and Whole Exome Sequencing. Elsevier, 2020.