ABCA3 Gene Mutations in Newborns with Fatal Surfactant Deficiency

New England Journal of Medicine

Volumn 350, Issue 13, 2004, Pages 1296-1303

  Shulenin, Sergey ^a   Nogee, Lawrence M ^b   Annilo, Tarmo ^a   Wert, Susan E ^c   Whitsett, Jeffrey A ^c   Dean, Michael ^a  

^a NATIONAL CANCER INSTITUTE   (United States)

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

^c UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; ABC TRANSPORTER A1; ABC TRANSPORTER A3; ABC TRANSPORTER A4; DNA; LIPID; LUNG SURFACTANT; PHOSPHOLIPID; PROTEIN; UNCLASSIFIED DRUG;

AIRWAY; ARTICLE; CLINICAL ARTICLE; ELECTRON MICROSCOPY; ETHNOLOGY; EXOCYTOSIS; EXON; FEMALE; FRAMESHIFT MUTATION; GENE MUTATION; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; INFANT; LAMELLAR BODY; LUNG ALVEOLUS CELL TYPE 2; LUNG DISEASE; LUNG FUNCTION; LUNG SURFACTANT DEFICIENCY; MACROPHAGE; MALE; MISSENSE MUTATION; NONSENSE MUTATION; PHOTORECEPTOR CELL; PHYLOGENY; PRIORITY JOURNAL; RACE;

ATP-BINDING CASSETTE TRANSPORTERS; BASE SEQUENCE; DNA MUTATIONAL ANALYSIS; EVOLUTION; FEMALE; HUMANS; INFANT, NEWBORN; MALE; MUTATION; PEDIGREE; PHOSPHOLIPIDS; POLYMORPHISM, GENETIC; PULMONARY ALVEOLI; PULMONARY SURFACTANT-ASSOCIATED PROTEINS; RESPIRATORY DISTRESS SYNDROME, NEWBORN;

EID: 1642400686     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJMoa032178     Document Type: Article

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