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AD hyper-IgE syndrome due to a novel loss-of-function mutation in STAT3 : a diagnostic pursuit won by clinical acuity

Author
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

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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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