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  2. Details for: MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity.
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MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. [electronic resource]

By:
  • Müller, Thomas
Contributor(s):
  • Hess, Michael W
  • Schiefermeier, Natalia
  • Pfaller, Kristian
  • Ebner, Hannes L
  • Heinz-Erian, Peter
  • Ponstingl, Hannes
  • Partsch, Joachim
  • Röllinghoff, Barbara
  • Köhler, Henrik
  • Berger, Thomas
  • Lenhartz, Henning
  • Schlenck, Barbara
  • Houwen, Roderick J
  • Taylor, Christopher J
  • Zoller, Heinz
  • Lechner, Silvia
  • Goulet, Olivier
  • Utermann, Gerd
  • Ruemmele, Frank M
  • Huber, Lukas A
  • Janecke, Andreas R
Producer: 20081030Description: 1163-5 p. digitalISSN:
  • 1546-1718
Subject(s):
  • Cell Polarity -- physiology
  • Codon, Nonsense -- genetics
  • Enterocytes -- pathology
  • Epithelium -- pathology
  • Female
  • Genetic Linkage
  • Genome, Human
  • Homozygote
  • Humans
  • Inclusion Bodies
  • Infant
  • Male
  • Microvilli -- pathology
  • Mutation, Missense -- genetics
  • Myosin Heavy Chains -- genetics
  • Myosin Type V -- genetics
  • Receptors, Transferrin -- genetics
Online resources:
  • Available from publisher's website
In: Nature genetics vol. 40
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity.

APA

Müller T., Hess M. W., Schiefermeier N., Pfaller K., Ebner H. L., Heinz-Erian P., Ponstingl H., Partsch J., Röllinghoff B., Köhler H., Berger T., Lenhartz H., Schlenck B., Houwen R. J., Taylor C. J., Zoller H., Lechner S., Goulet O., Utermann G., Ruemmele F. M., Huber L. A. & Janecke A. R. (20081030). MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. : Nature genetics.

Chicago

Müller Thomas, Hess Michael W, Schiefermeier Natalia, Pfaller Kristian, Ebner Hannes L, Heinz-Erian Peter, Ponstingl Hannes, Partsch Joachim, Röllinghoff Barbara, Köhler Henrik, Berger Thomas, Lenhartz Henning, Schlenck Barbara, Houwen Roderick J, Taylor Christopher J, Zoller Heinz, Lechner Silvia, Goulet Olivier, Utermann Gerd, Ruemmele Frank M, Huber Lukas A and Janecke Andreas R. 20081030. MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. : Nature genetics.

Harvard

Müller T., Hess M. W., Schiefermeier N., Pfaller K., Ebner H. L., Heinz-Erian P., Ponstingl H., Partsch J., Röllinghoff B., Köhler H., Berger T., Lenhartz H., Schlenck B., Houwen R. J., Taylor C. J., Zoller H., Lechner S., Goulet O., Utermann G., Ruemmele F. M., Huber L. A. and Janecke A. R. (20081030). MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. : Nature genetics.

MLA

Müller Thomas, Hess Michael W, Schiefermeier Natalia, Pfaller Kristian, Ebner Hannes L, Heinz-Erian Peter, Ponstingl Hannes, Partsch Joachim, Röllinghoff Barbara, Köhler Henrik, Berger Thomas, Lenhartz Henning, Schlenck Barbara, Houwen Roderick J, Taylor Christopher J, Zoller Heinz, Lechner Silvia, Goulet Olivier, Utermann Gerd, Ruemmele Frank M, Huber Lukas A and Janecke Andreas R. MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. : Nature genetics. 20081030.

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