Associated Papers
Novel insights into congenital surfactant dysfunction disorders by in silico analysis of ABCA3 proteins.
Xiao GL et al.
World Journal of Pediatrics : Wjp, 2023
A Term Neonatal Case With Lethal Respiratory Failure Associated With a Novel Homozygous Mutation in ABCA3 Gene.
Wei M et al.
Frontiers in Pediatrics, 2020
Heterozygosity for E292V in ABCA3, lung function and COPD in 64,000 individuals.
Bækvad-Hansen M et al.
Respiratory Research, 2012
22866751 (PubMed )
Supplement: 1465-9921-13-67-S4.doc
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