AD hyper-IgE syndrome due to a novel loss-of-function mutation in STAT3 : a diagnostic pursuit won by clinical acuity
- Author
- Leen Moens, Heidi Schaballie (UGent) , Barbara Bosch, Arnout Voet, Xavier Bossuyt, Jean-Laurent Casanova, Stephanie Boisson-Dupuis, Stuart G. Tangye and Isabelle Meyts
- Organization
- Keywords
- Autosomal dominant hyper-IgE syndrome, STAT3, unconventional Tcells, autism, CHRONIC MUCOCUTANEOUS CANDIDIASIS, T-CELLS, KEY FINDINGS, DEFICIENCY, IMMUNITY, IL-17, CHROMOSOME, CHILDREN, DELETION, ALBICANS
Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-01J82GQDSAC77282CC3BFGG4DM
- MLA
- Moens, Leen, et al. “AD Hyper-IgE Syndrome Due to a Novel Loss-of-Function Mutation in STAT3 : A Diagnostic Pursuit Won by Clinical Acuity.” JOURNAL OF CLINICAL IMMUNOLOGY, vol. 37, no. 1, 2017, pp. 12–17, doi:10.1007/s10875-016-0351-9.
- APA
- Moens, L., Schaballie, H., Bosch, B., Voet, A., Bossuyt, X., Casanova, J.-L., … Meyts, I. (2017). AD hyper-IgE syndrome due to a novel loss-of-function mutation in STAT3 : a diagnostic pursuit won by clinical acuity. JOURNAL OF CLINICAL IMMUNOLOGY, 37(1), 12–17. https://doi.org/10.1007/s10875-016-0351-9
- Chicago author-date
- Moens, Leen, Heidi Schaballie, Barbara Bosch, Arnout Voet, Xavier Bossuyt, Jean-Laurent Casanova, Stephanie Boisson-Dupuis, Stuart G. Tangye, and Isabelle Meyts. 2017. “AD Hyper-IgE Syndrome Due to a Novel Loss-of-Function Mutation in STAT3 : A Diagnostic Pursuit Won by Clinical Acuity.” JOURNAL OF CLINICAL IMMUNOLOGY 37 (1): 12–17. https://doi.org/10.1007/s10875-016-0351-9.
- Chicago author-date (all authors)
- Moens, Leen, Heidi Schaballie, Barbara Bosch, Arnout Voet, Xavier Bossuyt, Jean-Laurent Casanova, Stephanie Boisson-Dupuis, Stuart G. Tangye, and Isabelle Meyts. 2017. “AD Hyper-IgE Syndrome Due to a Novel Loss-of-Function Mutation in STAT3 : A Diagnostic Pursuit Won by Clinical Acuity.” JOURNAL OF CLINICAL IMMUNOLOGY 37 (1): 12–17. doi:10.1007/s10875-016-0351-9.
- Vancouver
- 1.Moens L, Schaballie H, Bosch B, Voet A, Bossuyt X, Casanova J-L, et al. AD hyper-IgE syndrome due to a novel loss-of-function mutation in STAT3 : a diagnostic pursuit won by clinical acuity. JOURNAL OF CLINICAL IMMUNOLOGY. 2017;37(1):12–7.
- IEEE
- [1]L. Moens et al., “AD hyper-IgE syndrome due to a novel loss-of-function mutation in STAT3 : a diagnostic pursuit won by clinical acuity,” JOURNAL OF CLINICAL IMMUNOLOGY, vol. 37, no. 1, pp. 12–17, 2017.
@article{01J82GQDSAC77282CC3BFGG4DM, author = {{Moens, Leen and Schaballie, Heidi and Bosch, Barbara and Voet, Arnout and Bossuyt, Xavier and Casanova, Jean-Laurent and Boisson-Dupuis, Stephanie and Tangye, Stuart G. and Meyts, Isabelle}}, issn = {{0271-9142}}, journal = {{JOURNAL OF CLINICAL IMMUNOLOGY}}, keywords = {{Autosomal dominant hyper-IgE syndrome,STAT3,unconventional Tcells,autism,CHRONIC MUCOCUTANEOUS CANDIDIASIS,T-CELLS,KEY FINDINGS,DEFICIENCY,IMMUNITY,IL-17,CHROMOSOME,CHILDREN,DELETION,ALBICANS}}, language = {{eng}}, number = {{1}}, pages = {{12--17}}, title = {{AD hyper-IgE syndrome due to a novel loss-of-function mutation in STAT3 : a diagnostic pursuit won by clinical acuity}}, url = {{http://doi.org/10.1007/s10875-016-0351-9}}, volume = {{37}}, year = {{2017}}, }
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