ABCA3 Gene Mutations in Newborns with Fatal Surfactant Deficiency
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ABCA3 mutations associated with pediatric interstitial lung disease
DOI 10.1164/rccm.200503-504OC
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Clinical, radiological and pathological features of ABCA3 mutations in children
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Surfactant composition and function in patients with ABCA3 mutations
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Identification of LBM180, a lamellar body limiting membrane protein of alveolar type II cells, as the ABC transporter protein ABCA3
DOI 10.1074/jbc.M201812200
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