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Dive into the research topics of 'Phenotypic and clinical heterogeneity associated with monoallelic TNFRSF13B-A181E mutations in common variable immunodeficiency'. Together they form a unique fingerprint.- Sort by
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Xiangyang Dong, Michelle V. Hoeltzle, John B. Hagan, Miguel A. Park, James T. Li, Roshini S. Abraham
Research output: Contribution to journal › Article › peer-review