SFTPC gene mutation p.R167Q in a premature infant. [electronic resource]
Producer: 20141022Description: E66-8 p. digitalISSN:- 1099-0496
- Anti-Inflammatory Agents -- therapeutic use
- Bronchopulmonary Dysplasia -- complications
- Disease Progression
- Humans
- Infant, Extremely Premature
- Infant, Newborn
- Male
- Mutation
- Pulmonary Alveolar Proteinosis -- complications
- Pulmonary Surfactant-Associated Protein C -- deficiency
- Respiration, Artificial
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Publication Type: Case Reports; Journal Article
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