Child Interstitial Lung Disease in an Infant with Surfactant Protein C Dysfunction due to c.202G>T Variant (p.V68F)
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pulmonary and Respiratory Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00408-021-00501-2.pdf
Reference17 articles.
1. Kuo CS, Young LR (2014) Interstitial lung disease in children. Curr Opin Pediatr 26(3):320–327. https://doi.org/10.1097/MOP.0000000000000094
2. Kurland G, Deterding RR, Hagood JS, Young LR, Brody AS, Castile RG et al (2013) An official American thoracic society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy. Am J Respir Crit Care Med 188(3):376–394. https://doi.org/10.1164/rccm.201305-0923ST
3. Willander H, Askarieh G, Landreh M, Westermark P, Nordling K, Keranen H et al (2012) High-resolution structure of a BRICHOS domain and its implications for anti-amyloid chaperone activity on lung surfactant protein C. Proc Natl Acad Sci U S A 109(7):2325–2329. https://doi.org/10.1073/pnas.1114740109
4. Spagnolo P, Bush A (2016) Interstitial lung disease in children younger than 2 years. Pediatrics. https://doi.org/10.1542/peds.2015-2725
5. Wert SE, Whitsett JA, Nogee LM (2009) Genetic disorders of surfactant dysfunction. Pediatr Dev Pathol 12(4):253–274. https://doi.org/10.2350/09-01-0586.1
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1. LUNG Year in Review: 2022;Lung;2023-01-30
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