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...

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Detalles Bibliográficos
Autores principales: Li, Wang, Long, Chen, Renjun, Li, Zhangxue, Hu, Yin, Hu, Wanwei, Li, Juan, Ma, Yuan, Shi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661423/
https://www.ncbi.nlm.nih.gov/pubmed/26611714
http://dx.doi.org/10.1038/srep17317

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661423/
https://www.ncbi.nlm.nih.gov/pubmed/26611714
http://dx.doi.org/10.1038/srep17317

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