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Human Mutation
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February 27, 2010
Loss-of-function of MYO5B is the main cause of microvillus inclusion disease: 15 novel mutations and a CaCo-2 RNAi cell model
Frank M Ruemmele, Thomas Müller, Natalia Schiefermeier, et al.
Gastroenterology
|
April 15, 2014
Loss of syntaxin 3 causes variant microvillus inclusion disease
Caroline L Wiegerinck, Andreas R Janecke, Kerstin Schneeberger, et al.
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Search research articles
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Showing results (61-70 of 62) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 62 results.
Human Mutation
|
February 27, 2010
Loss-of-function of MYO5B is the main cause of microvillus inclusion disease: 15 novel mutations and a CaCo-2 RNAi cell model
Frank M Ruemmele, Thomas Müller, Natalia Schiefermeier, et al.
Gastroenterology
|
April 15, 2014
Loss of syntaxin 3 causes variant microvillus inclusion disease
Caroline L Wiegerinck, Andreas R Janecke, Kerstin Schneeberger, et al.
Page
of 7