POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss（次世代シーケンサーにより見出された日本人難聴患者におけるPOU4F3遺伝子変異）

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POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss（次世代シーケンサーにより見出された日本人難聴患者におけるPOU4F3遺伝子変異）

Persistent ID (NDL): info:ndljp/pid/11122904

Material type: 博士論文

Author: 北野, 友裕

Publisher: 信州大学

Date granted: 2017-03-31

Material Format: Digital

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Degree grantor and degree: 信州大学(Shinshu university),博士（医学）

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Note (General)：: 出版タイプ： NA雑誌に発表。PLOS ONE. 12(5):e0177636 (2017); doi:10.1371/journal.pone.0177636.Thesis...

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Material Type: 博士論文
Title: POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss（次世代シーケンサーにより見出された日本人難聴患者におけるPOU4F3遺伝子変異）
Author/Editor: 北野, 友裕
Author Heading: 北野, 友裕
Publication, Distribution, etc.: 信州大学
Publication Date: 2017-03-31
Publication Date (W3CDTF): 2017-03-31
Degree Grantor: 信州大学(Shinshu university)
Date Granted: 2017-03-31
Date Granted (W3CDTF): 2017-03-31
Dissertation Number: 13601甲第1106号
Degree Type: 博士（医学）
Conferring No. (Dissertation): 甲第1106号
Text Language Code: eng
Target Audience: 一般
Note (General): 出版タイプ： NA
雑誌に発表。PLOS ONE. 12(5):e0177636 (2017); doi:10.1371/journal.pone.0177636.
Thesis
北野　友裕. POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss（次世代シーケンサーにより見出された日本人難聴患者におけるPOU4F3遺伝子変異）. 信州大学, 2017, 博士論文.
機関リポジトリ記載の権利情報: © 2017 Kitano et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. / Kitano T, Miyagawa M, Nishio S-y, Moteki H, Oda K, Ohyama K, et al. (2017) POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss. PLoS ONE 12(5): e0177636. https://doi.org/10.1371/journal.pone.0177636
Persistent ID (NDL): info:ndljp/pid/11122904
https://dl.ndl.go.jp/pid/11122904
Collection: 障害者向け資料
Collection (Materials For Handicapped People:1): テキストデータ
Collection (particular): 国立国会図書館デジタルコレクション > デジタル化資料 > 博士論文
https://dl.ndl.go.jp/collections/A00014
Acquisition Basis: 博士論文（自動収集）
Date Accepted (W3CDTF): 2018-08-03T23:36:01+09:00
Format (IMT): application/pdf
Access Restrictions: 国立国会図書館内限定公開
Service for the Digitized Contents Transmission Service: 図書館・個人送信対象外
Availability of remote photoduplication service: 可
Related Material (URI): https://doi.org/10.1371/journal.pone.0177636
Periodical Title (URI): http://hdl.handle.net/10091/00020712
Data Provider (Database): 国立国会図書館 : 国立国会図書館デジタルコレクション
https://dl.ndl.go.jp

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