Associated Papers
Clinical characteristics of SFTPC gene mutations in children: a single-center experience.
Yang T et al.
Italian Journal of Pediatrics, 2025
40890883 (PubMed )
Supplement: 13052_2025_2101_MOESM3_ESM.doc
A Test to Comprehensively Capture the Known Genetic Component of Familial Pulmonary Fibrosis.
Villeneuve J et al.
American Journal of Respiratory Cell and Molecular Biology, 2024
Recurrent diffuse lung disease due to surfactant protein C deficiency.
Kazzi B et al.
Respiratory Medicine Case Reports, 2018
A novel surfactant protein C gene mutation associated with progressive respiratory failure in infancy.
Litao MK et al.
Pediatric Pulmonology, 2017
Genome sequencing of idiopathic pulmonary fibrosis in conjunction with a medical school human anatomy course.
Kumar A et al.
Plos One, 2014
Surfactant protein C gene (SFTPC) mutation-associated lung disease: high-resolution computed tomography (HRCT) findings and its relation to histological analysis.
Mechri M et al.
Pediatric Pulmonology, 2010
Characteristics of disorders associated with genetic mutations of surfactant protein C.
Thouvenin G et al.
Archives of Disease in Childhood, 2010
New surfactant protein C gene mutations associated with diffuse lung disease.
Guillot L et al.
Journal of Medical Genetics, 2009
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