Population
A child with congenital microvillus atrophy, alongside normal and disease controls
Comparison
Analysis of brush border membrane proteins by… vs Brush border membrane proteins from normal and…
Design
Case_report
Authors
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May identify a candidate defect in congenital microvillus atrophy; hypothesis-generating and requires confirmation before clinical relevance.
A diminished 200K MW brush border membrane protein band may be the underlying defect causing involution of microvilli in congenital microvillus atrophy.
Carruthers et al. (1985) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: