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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...
Gardado en:
| Publicado en: | Sci Rep |
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| Main Authors: | , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Nature Publishing Group
2015
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| Assuntos: | |
| Acceso en liña: | 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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