MYO5B mutations in patients with microvillus inclusion disease presenting with transient renal Fanconi syndrome.

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Published in J Pediatr Gastroenterol Nutr on April 01, 2012

Authors

Magdalena R Golachowska1, Carin M L van Dael, Hilda Keuning, Arend Karrenbeld, Dick Hoekstra, Carolien F M Gijsbers, Marc A Benninga, Edmond H H M Rings, Sven C D van Ijzendoorn

Author Affiliations

1: Department of Cell Biology, Section of Membrane Cell Biology, University Medical Center Groningen, University of Groningen, The Netherlands.

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