Ding, F., Wu, C., Li, Y., Mukherjee, S., Ghosh, S., Arrossi, A. V., & Krishnan, S. (2021). A case of hypereosinophilic syndrome with STAT5b N642H mutation. Oxf Med Case Reports.
Citación estilo ChicagoDing, Feihong, Chaoping Wu, Yun Li, Sudipto Mukherjee, Subha Ghosh, A Valeria Arrossi, y Sudhir Krishnan. "A Case of Hypereosinophilic Syndrome With STAT5b N642H Mutation." Oxf Med Case Reports 2021.
Cita MLADing, Feihong, et al. "A Case of Hypereosinophilic Syndrome With STAT5b N642H Mutation." Oxf Med Case Reports 2021.
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