Familial pulmonary alveolar proteinosis and type I interferonopathy by mutation of STAT2 (TIMS2)

Journal of Experimental Medicine · Published 2026-07-16 · DOI 10.1084/jem.20251331

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Authors (41)

Conor Gruber, Meredith Ramba, Bineeta Debnath, Lorenzo Cuollo, Anna-Lena Neehus, Angelica Lee, Sofija Buta, Marta Martin-Fernandez, Jérémie Rosain, Laureline Berteloot, Philippe Drabent, Tom Le Voyer, Camille Soudée, Jessica N. Peel, Yoann Seeleuthner, Anne Puel, Shen-Ying Zhang, Michael J. Ciancanelli, Carlos A. Arango-Franco, Mélanie Migaud, Marie-Louise Frémond, Florence Renaldo, Odile Boespflug-Tanguy, Imen Dorboz, Beatrice Dubern, Tristan Fonteneau, Nima Parvaneh, Rasol Molatefi, Mohammad Shahrooei, Darragh Duffy, Vincent Bondet, Gillian I. Rice, Yanick J. Crow, Thierry Jo Molina, Nathalie Boddaert, Jean-Laurent Casanova, Veronique Houdouin, Isabelle Melki, Alice Hadchouel, Jacinta Bustamante, Dusan Bogunovic

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Year
2026

Citation

Gruber, C., Ramba, M., Debnath, B., et al. (2026). Familial pulmonary alveolar proteinosis and type I interferonopathy by mutation of STAT2 (TIMS2). Journal of Experimental Medicine. https://doi.org/10.1084/jem.20251331

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