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遺伝子解析に基づいた難聴発症メカニズムの解明および個別化医療システムの構築
http://hdl.handle.net/10091/00021700
c8525b8d-267d-486d-b2cc-796858cf9f01
名前 / ファイル | ライセンス | アクション | |
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Item type | 研究報告書 / Research Paper(1) | |||||
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公開日 | 2019-10-24 | |||||
タイトル | ||||||
言語 | ja | |||||
タイトル | 遺伝子解析に基づいた難聴発症メカニズムの解明および個別化医療システムの構築 | |||||
言語 | ||||||
言語 | jpn | |||||
資源タイプ | ||||||
資源 | http://purl.org/coar/resource_type/c_18ws | |||||
タイプ | research report | |||||
その他(別言語等)のタイトル | ||||||
その他のタイトル | Development of high throughput sequencing analysis based system for personalized medicine of deafness | |||||
著者 |
宇佐美, 真一
× 宇佐美, 真一 |
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信州大学研究者総覧へのリンク | ||||||
氏名 | 宇佐美, 真一 | |||||
URL | http://soar-rd.shinshu-u.ac.jp/profile/ja.ZmAUHUSC.html | |||||
引用 | ||||||
内容記述タイプ | Other | |||||
内容記述 | 2015~2017年度科学研究費助成事業(基盤研究(A))研究成果報告書 課題番号:15H02565 研究代表者:宇佐美 真一 | |||||
書誌情報 |
発行日 2018 |
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内容記述 | ||||||
内容記述タイプ | Other | |||||
内容記述 | 研究種目:基盤研究(A) | |||||
内容記述 | ||||||
内容記述タイプ | Other | |||||
内容記述 | 研究期間:2015~2017 | |||||
内容記述 | ||||||
内容記述タイプ | Other | |||||
内容記述 | 課題番号:15H02565 | |||||
内容記述 | ||||||
内容記述タイプ | Other | |||||
内容記述 | 研究代表者:宇佐美 真一 | |||||
内容記述 | ||||||
内容記述タイプ | Other | |||||
内容記述 | 研究者番号:10184996 | |||||
資源タイプ(コンテンツの種類) | ||||||
内容記述タイプ | Other | |||||
内容記述 | Other | |||||
出版タイプ | ||||||
出版タイプ | VoR | |||||
出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 |