Myo5b knockout mice as a model of microvillus inclusion disease

Inherited MYO5B mutations have recently been associated with microvillus inclusion disease (MVID), an autosomal recessive syndrome characterized by intractable, life-threatening, watery diarrhea appearing shortly after birth. Characterization of the molecular mechanisms underlying this disease and d...

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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Cartón-García, Fernando, Overeem, Arend W., Nieto, Rocio, Bazzocco, Sarah, Dopeso, Higinio, Macaya, Irati, Bilic, Josipa, Landolfi, Stefania, Hernandez-Losa, Javier, Schwartz, Simo, Ramon y Cajal, Santiago, van Ijzendoorn, Sven C. D., Arango, Diego
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2015
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4511872/
https://ncbi.nlm.nih.gov/pubmed/26201991
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep12312
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