Human inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.
- DOI
- 10.1084/jem.20252038
- Published
- 2026 Oct 5
- Container
- The Journal of experimental medicine
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1084/jem.20252038,
title = {Human inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.},
author = {Fagniez I and Tsumura M and Guérin A and Abolhassani H and Sharafian S and Mesdaghi M and Nishimura T and Lashkari HP and Rao S and Richards S and Han JE and Delmonte OM and Kergaravat C and Markle JG and Ogishi M and Han J and Peel J and Vellutini J and Feng Y and Soudée C and Migaud M and Palterer B and Jackson KJL and Nishimura S and Sakata S and Kinoshita K and Yamamoto A and Moritake H and Alzahrani M and Vallejos F and Cole T and Smart JM and Choo S and Chavoshzadeh Z and Armin S and Toubert A and Zhang P and Rosain J and Notarangelo LD and Pan-Hammarström Q and Tangye SG and Casanova JL and Ma CS and Puel A and Bustamante J and Okada S and Boisson-Dupuis S and Yang R},
year = {2026},
journal = {The Journal of experimental medicine},
doi = {10.1084/jem.20252038},
url = {https://doi.org/10.1084/jem.20252038}
}RIS
TY - JOUR TI - Human inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity. AU - Fagniez I AU - Tsumura M AU - Guérin A AU - Abolhassani H AU - Sharafian S AU - Mesdaghi M AU - Nishimura T AU - Lashkari HP AU - Rao S AU - Richards S AU - Han JE AU - Delmonte OM AU - Kergaravat C AU - Markle JG AU - Ogishi M AU - Han J AU - Peel J AU - Vellutini J AU - Feng Y AU - Soudée C AU - Migaud M AU - Palterer B AU - Jackson KJL AU - Nishimura S AU - Sakata S AU - Kinoshita K AU - Yamamoto A AU - Moritake H AU - Alzahrani M AU - Vallejos F AU - Cole T AU - Smart JM AU - Choo S AU - Chavoshzadeh Z AU - Armin S AU - Toubert A AU - Zhang P AU - Rosain J AU - Notarangelo LD AU - Pan-Hammarström Q AU - Tangye SG AU - Casanova JL AU - Ma CS AU - Puel A AU - Bustamante J AU - Okada S AU - Boisson-Dupuis S AU - Yang R PY - 2026 JO - The Journal of experimental medicine DO - 10.1084/jem.20252038 UR - https://doi.org/10.1084/jem.20252038 ER -
APA
I, F., M, T., A, G., H, A., S, S., M, M., T, N., HP, L., S, R., S, R., JE, H., OM, D., C, K., JG, M., M, O., J, H., J, P., J, V., Y, F., C, S., M, M., B, P., KJL, J., S, N., S, S., K, K., A, Y., H, M., M, A., F, V., T, C., JM, S., S, C., Z, C., S, A., A, T., P, Z., J, R., LD, N., Q, P., SG, T., JL, C., CS, M., A, P., J, B., S, O., S, B., & R, Y. (2026). Human inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.. The Journal of experimental medicine. https://doi.org/10.1084/jem.20252038
Source records
- pubmed · retrieved 2026-09-25T04:13:59.547Z