Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome. [electronic resource]
Producer: 20130204Description: e1575-82 p. digitalISSN:- 1098-4275
- 1-Acylglycerophosphocholine O-Acyltransferase -- genetics
- ATP-Binding Cassette Transporters -- genetics
- Black or African American -- genetics
- Choline-Phosphate Cytidylyltransferase -- genetics
- Cohort Studies
- Diacylglycerol Cholinephosphotransferase -- genetics
- Exome -- genetics
- Gene Expression Regulation -- genetics
- Genetic Association Studies
- Genetic Predisposition to Disease -- ethnology
- Gestational Age
- Heterozygote
- Homozygote
- Humans
- Infant, Newborn
- Mutation
- Pulmonary Surfactant-Associated Protein C -- genetics
- Respiratory Distress Syndrome, Newborn -- ethnology
- Risk
- White People -- genetics
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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