Genetic mechanisms of surfactant deficiency

Biology of the Neonate

Volumn 85, Issue 4, 2004, Pages 314-318

  Nogee, Lawrence M ^a,b  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b JOHNS HOPKINS HOSPITAL   (United States)

Author keywords

Alveolar proteinosis; Infant, newborn; Interstitial lung disease; Mutation; Pulmonary surfactants; Respiratory distress syndrome

Indexed keywords

LUNG SURFACTANT; PROTEIN; PROTEIN ABCA 3; SURFACTANT PROTEIN B; SURFACTANT PROTEIN C; UNCLASSIFIED DRUG;

ACUTE DISEASE; CHROMOSOME 2; CHRONIC LUNG DISEASE; CLINICAL FEATURE; CONFERENCE PAPER; GENE; GENE MUTATION; GENETIC CODE; GENETIC DISORDER; HEREDITARY SURFACTANT PROTEIN B DEFICIENCY; HUMAN; LABORATORY TEST; LUNG ALVEOLUS; LUNG ALVEOLUS SURFACE TENSION; LUNG DISEASE; LUNG FUNCTION; METABOLISM; MISSENSE MUTATION; MOLECULAR MECHANICS; NONHUMAN; PRIORITY JOURNAL; PROTEIN ABCA 3 DEFICIENCY; PROTEIN DEFICIENCY; PROTEIN SYNTHESIS; RNA SPLICING; SURFACTANT DEFICIENCY;

ATP-BINDING CASSETTE TRANSPORTERS; HUMANS; INFANT, NEWBORN; LUNG DISEASES; MUTATION; PULMONARY SURFACTANT-ASSOCIATED PROTEIN B; PULMONARY SURFACTANT-ASSOCIATED PROTEIN C; PULMONARY SURFACTANT-ASSOCIATED PROTEINS; PULMONARY SURFACTANTS; RESPIRATORY DISTRESS SYNDROME, NEWBORN;

EID: 3042663294     PISSN: 00063126     EISSN: None     Source Type: Journal    
DOI: 10.1159/000078171     Document Type: Conference Paper

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