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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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| 出版年: | Physiol Rep |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley and Sons Inc.
2016
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| 主題: | |
| オンライン･アクセス: | 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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