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Published in 2018 at "Pediatric Research"
DOI: 10.1038/pr.2018.30
Abstract: BackgroundMutations in the NK2 homeobox 1 (NKX2-1) gene are associated with lung disease in infants and children. We hypothesize that disruption of normal surfactant gene expression with these mutations contributes to the respiratory phenotypes observed.MethodsTo…
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Keywords:
gene;
sftpb sftpc;
expression;
mutations thyroid ... See more keywords