Inherited Surfactant Deficiency Caused by Uniparental Disomy of Rare Mutations in the Surfactant Protein-B and ATP Binding Cassette, Subfamily A, Member 3 Genes
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Supported by the National Heart, Lung, and Blood Institute (HL 65174 and HL 82747-FSC/AH, HL 54703) (L.M.N.), the Eudowood Foundation (L.M.N.), and the Children's Discovery Institute and the Saigh Foundation (F.S.C., A.H.).
The authors declare no conflicts of interest.
PII: S0022-3476(09)00551-4
doi:10.1016/j.jpeds.2009.06.006
© 2009 Mosby, Inc. All rights reserved.
