Interstitial lung disease in children – genetic background and associated phenotypesPediatric Pneumology, Childrens' hospital of the Ludwig-Maximilians-University, Munich, Germany
Respiratory Research 2005, 6:32doi:10.1186/1465-9921-6-32
Additional filesAdditional File 1: Table 1. Pathological features and clinical phenotypes of reported cases with partial SP-B deficiency. Table 2. Pathological features and clinical phenotypes of reported cases with mutations in the SP-C gene. Table 3. Overview: Pediatric interstitial lung disease associated with surfactant protein deficiency or ABCA3 mutations Format: DOC Size: 149KB Download file This file can be viewed with: Microsoft Word Viewer |




on Google Scholar







author email
corresponding author email