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microvillus
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Curated Studies
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OMIM - Urogenital and Digestive Disorders
OMIM - Microvillus inclusion disease
Pluripotent stem cells wildtype or podocalyxin (PODXL) mutants
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Literature
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Analysis of a child with Microvillus inclusion disease due to variants of MYO5B gene and a literatur…
Patient-derived enteroids provide a platform for the development of therapeutic approaches in microv…
Two cases of microvillus inclusion disease caused by MYO5B deficiency with prenatal abnormalities.
Pathogenic STX3 variants affecting the retinal and intestinal transcripts cause an early-onset sever…
UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-depende…
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Evaluation of Intestinal Brush Border Enzyme Function in Critically Ill Patients
Amino Acid-based Oral Rehydration Solution in Children With Short Bowel Syndrome
Prevention of Parenteral Nutrition-Associated Cholestasis With Cyclic Parenteral Nutrition in Infant…
Safety and Dosing Study of Glucagon-like Peptide 2 (GLP-2) in Infants and Children With Intestinal F…
A 90 Day, Phase 4,Open Labeled Exploratory Study of RELiZORB
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