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RNA‐sequencing of WFS1‐deficient pancreatic islets
Wolfram syndrome, an autosomal recessive disorder characterized by juvenile‐onset diabetes mellitus and optic atrophy, is caused by mutations in the WFS1 gene. WFS1 encodes an endoplasmic reticulum resident transmembrane protein. The Wfs1‐null mice exhibit progressive insulin deficiency and diabetes...
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| Publicado no: | Physiol Rep |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4831324/ https://ncbi.nlm.nih.gov/pubmed/27053292 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14814/phy2.12750 |
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