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Functional characterization of mutations in the myosin Vb gene associated with microvillus inclusion disease.
J Pediatr Gastroenterol Nutr. 2011 Mar;52(3):307-13. doi: 10.1097/MPG.0b013e3181eea177.
J Pediatr Gastroenterol Nutr. 2011.
PMID: 21206382
Free PMC article.
MYO5B mutations in patients with microvillus inclusion disease presenting with transient renal Fanconi syndrome.
Golachowska MR, van Dael CM, Keuning H, Karrenbeld A, Hoekstra D, Gijsbers CF, Benninga MA, Rings EH, van Ijzendoorn SC.
Golachowska MR, et al.
J Pediatr Gastroenterol Nutr. 2012 Apr;54(4):491-8. doi: 10.1097/MPG.0b013e3182353773.
J Pediatr Gastroenterol Nutr. 2012.
PMID: 22441677
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Recycling endosomes in apical plasma membrane domain formation and epithelial cell polarity.
Golachowska MR, Hoekstra D, van IJzendoorn SC.
Golachowska MR, et al.
Trends Cell Biol. 2010 Oct;20(10):618-26. doi: 10.1016/j.tcb.2010.08.004.
Trends Cell Biol. 2010.
PMID: 20833047
Review.
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