Functional Characterization of Mutations in the Myosin Vb Gene Associated With Microvillus Inclusion Disease-Reference-Cited by-同舟云学术

Functional Characterization of Mutations in the Myosin Vb Gene Associated With Microvillus Inclusion Disease

Published:2011-03 Issue:3 Volume:52 Page:307-313
ISSN:0277-2116
Container-title:Journal of Pediatric Gastroenterology & Nutrition
language:en
Short-container-title:

Author:

Szperl Agata M,Golachowska Magdalena R,Bruinenberg Marcel,Prekeris Rytis,Thunnissen Andy-Mark WH,Karrenbeld Arend,Dijkstra Gerard,Hoekstra Dick,Mercer David,Ksiazyk Janusz,Wijmenga Cisca,Wapenaar Martin C,Rings Edmond HHM,van IJzendoorn Sven CD

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology,Pediatrics, Perinatology, and Child Health

Reference24 articles.

1. Congenital microvillous atrophy: specific diagnostic features;Phillips;Arch Dis Child,1985

2. Familial microvillous atrophy: a clinicopathological survey of 23 cases;Phillips;J Pediatr Gastroenterol Nutr,1992

3. Microvillus inclusion disease: an inherited defect of brush-border assembly and differentiation;Cutz;N Engl J Med,1989

4. Neonatal enteropathies: defining the causes of protracted diarrhea of infancy;Sherman;J Pediatr Gastroenterol Nutr,2004

5. Irreversible intestinal failure;Goulet;J Pediatr Gastroenterol Nutr,2004

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