Association of SCNN1A Single Nucleotide Polymorphisms with neonatal respiratory distress syndrome
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چکیده
منابع مشابه
Association of SCNN1A Single Nucleotide Polymorphisms with neonatal respiratory distress syndrome
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-co...
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ژورنال
عنوان ژورنال: Scientific Reports
سال: 2015
ISSN: 2045-2322
DOI: 10.1038/srep17317