Alteration of the Pulmonary Surfactant System in Full-Term Infants with Hereditary ABCA3 Deficiency-Reference-Cited by-同舟云学术

Alteration of the Pulmonary Surfactant System in Full-Term Infants with Hereditary ABCA3 Deficiency

Published:2006-09 Issue:5 Volume:174 Page:571-580
ISSN:1073-449X
Container-title:American Journal of Respiratory and Critical Care Medicine
language:en
Short-container-title:Am J Respir Crit Care Med

Author:

Brasch Frank,Schimanski Sven,Mühlfeld Christian,Barlage Stefan,Langmann Thomas,Aslanidis Charalampos,Boettcher Alfred,Dada Ashraf,Schroten Horst,Mildenberger Eva,Prueter Eric,Ballmann Manfred,Ochs Matthias,Johnen Georg,Griese Matthias,Schmitz Gerd

Publisher

American Thoracic Society

Subject

Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine

Reference40 articles.

1. ABCA3Gene Mutations in Newborns with Fatal Surfactant Deficiency

2. The Human ATP-Binding Cassette (ABC) Transporter Superfamily

3. Structure, function and regulation of the ABC1 gene product

4. The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease

5. Mutation of the Stargardt Disease Gene ( ABCR ) in Age-Related Macular Degeneration

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