A mutation in the surfactant protein C gene associated with familial interstitial lung disease.

By L. Nogee, A. Dunbar, S. Wert, F. Askin, A. Hamvas, Jeffrey A. Whitsett. New England Journal of Medicine, 2001

872 citations recorded by the source corpus.

Subfields: Communication, Economics and Econometrics, Sociology and Political Science

View Paper: https://www.semanticscholar.org/paper/aee1f8f8eca54030fe820778561208cdf4b8d5a2

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Citations in the corpus

• TGF-β1 Signaling and Tissue Fibrosis. (2018, background): “Genetic analysis of patients with familial interstitial pneumonitis point to type II alveolar epithelial dysfunction as a consequence of SP gene mutations and as a causal mechanism for pulmonary fibrosis (Nogee et al. 2001; Thomas et al. 2002; Wang et al. 2009; Garcia 2011).”