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References and Further Reading
Cutz, E., Sherman, P. M., & Davidson, G. P. (1997). Enteropathies associated with protracted diarrhea of infancy: Clinicopathological features, cellular and molecular mechanisms. Pediatric Pathology & Laboratory Medicine, 17(3), 335–368.
Groisman, G. M., Amar, M., & Livne, E. (2002). CD10, a valuable tool for the light microscopic diagnosis of microvillous inclusion disease (familial microvillous atrophy). The American Journal of Surgical Pathology, 26(7), 902–907.
Khubchandani, S. R., Vohra, P., Chitale, A. R., & Sidana, P. (2011). Microvillous inclusion disease-an ultrastructural diagnosis: With a review of the literature. Ultrastructural Pathology, 35, 87–91.
Shaila, R. K., Pankaj, V., Arun, R. C., & Poonam, S. (2011). Microvillous inclusion disease-an ultrastructural diagnosis: With a review of the literature. Ultrastructural Pathology, 35, 87–91.
Szperl, A. M., Golachowska, M. R., Bruinenberg, M., Prekeris, R., Thunnissen, A. M., Karrenbeld, A., Dijkstra, G., Hoekstra, D., Mercer, D., Ksiazyk, J., Wijmenga, C., Wapenaar, M. C., Rings, E. H., & van IJzendoorn, S. C. (2011). Functional characterization of mutations in the myosin Vb gene associated with microvillus inclusion disease. Journal of Pediatric Gastroenterology and Nutrition, 52, 307–313.
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Ensari, A. (2017). Microvillous Inclusion Disease. In: Carneiro, F., Chaves, P., Ensari, A. (eds) Pathology of the Gastrointestinal Tract. Encyclopedia of Pathology. Springer, Cham. https://doi.org/10.1007/978-3-319-40560-5_1511
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DOI: https://doi.org/10.1007/978-3-319-40560-5_1511
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