Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome.

Wambach, Jennifer A

Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome. [electronic resource] - Pediatrics Dec 2012 - e1575-82 p. digital

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

1098-4275

10.1542/peds.2012-0918 doi


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