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Disruption of Slc52a3 gene causes neonatal lethality with riboflavin deficiency in mice
Homeostasis of riboflavin should be maintained by transporters. Previous in vitro studies have elucidated basic information about riboflavin transporter RFVT3 encoded by SLC52A3 gene. However, the contribution of RFVT3 to the maintenance of riboflavin homeostasis and the significance in vivo remain...
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| 出版年: | Sci Rep |
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| 主要な著者: | , , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Nature Publishing Group
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4897618/ https://ncbi.nlm.nih.gov/pubmed/27272163 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep27557 |
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