Associated Papers
Interstitial lung disease in a baby with a de novo mutation in the SFTPC gene.
Brasch F et al.
The European Respiratory Journal, 2004
Compound SFTPB 1549C-->GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency.
Tredano M et al.
Human Mutation, 1999
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