ABCA3 missense mutations causing surfactant dysfunction disorders have distinct cellular phenotypes
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Title
ABCA3 missense mutations causing surfactant dysfunction disorders have distinct cellular phenotypes
Authors
Keywords
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Journal
HUMAN MUTATION
Volume 39, Issue 6, Pages 841-850
Publisher
Wiley
Online
2018-03-06
DOI
10.1002/humu.23416
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Related references
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- (2014) Jennifer A. Wambach et al. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
- Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum
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- Aberrant catalytic cycle and impaired lipid transport into intracellular vesicles in ABCA3 mutants associated with nonfatal pediatric interstitial lung disease
- (2008) Yoshihiro Matsumura et al. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY
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