ABCA3 gene mutations shape the clinical profiles of severe unexplained respiratory distress syndrome in late preterm and term infants

BACKGROUND: The majority of unexplained respiratory distress syndrome (URDS) cases in late preterm and term infants are caused by genetic abnormalities, with the most common of these being ABCA3 gene mutation. At present, it is unclear to neonatologists whether URDS patients with ABCA3 mutation have...

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Detalles Bibliográficos
Autores principales: Wang, Jianhui, Fan, Juan, Zhang, Yuting, Huang, Lie, Shi, Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7944190/
https://www.ncbi.nlm.nih.gov/pubmed/33708521
http://dx.doi.org/10.21037/tp-20-283

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7944190/
https://www.ncbi.nlm.nih.gov/pubmed/33708521
http://dx.doi.org/10.21037/tp-20-283

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