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Article

Association of SCNN1A Single Nucleotide Polymorphisms with neonatal respiratory distress syndrome.

Scientific reports - 27 Nov 2015

Li Wang, Long Chen, Renjun Li, Zhangxue Hu, Yin Hu, Wanwei Li, Juan Ma, Yuan Shi

Abstract excerpt

Increasing evidence has demonstrated that lung fluid absorption disorders might be an important cause of neonatal respiratory distress syndrome (RDS) by influencing gas exchange or surfactant function. The SCNN1A gene, which encodes the α-ENaC, might predispose infants to RDS. To explore whether the single-nucleotide polymorphisms (SNPs) of SCNN1A are associated with RDS, we conducted a case-control study to...

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Identifiers

PMID: 26611714
DOI: 10.1038/srep17317
PMCID: PMC4661423

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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