自閉症で同定された希少なneuroligin1遺伝子変異の機能的意義

Material type: 博士論文

Author: 仲西, 萌絵

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Name of awarding university/degree: 広島大学,博士(医学),Doctor of Philosophy in Medical Science

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Nakanishi M, Nomura J, Ji X, Tamada K, Arai T, Takahashi E, et al. (2017) Functional significance of rare neuroligin 1 variants found in autism. PLoS Genet 13(8): e1006940.

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Material Type: 博士論文
Title: 自閉症で同定された希少なneuroligin1遺伝子変異の機能的意義
Author/Editor: 仲西, 萌絵
Author Heading: 仲西, 萌絵
Alternative Title: Functional significance of rare neuroligin 1 variants found in autism
Degree grantor/type: 広島大学
Date Granted: 2017-11-22
Dissertation Number: 乙第4336号
Degree Type: 博士(医学)
Doctor of Philosophy in Medical Science
Text Language Code: eng
Target Audience: 一般
Format (IMT): application/pdf
Source: fulltext
http://ir.lib.hiroshima-u.ac.jp/45973/files/746
Access Restrictions: インターネット公開
Rights (production): © 2017 Nakanishi 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.
Related Material: Nakanishi M, Nomura J, Ji X, Tamada K, Arai T, Takahashi E, et al. (2017) Functional significance of rare neuroligin 1 variants found in autism. PLoS Genet 13(8): e1006940.
Related Material (URI): URI
https://doi.org/10.1371/journal.pgen.1006940
Data Provider (Database): 国立情報学研究所 : 学術機関リポジトリデータベース（IRDB）（機関リポジトリ）
https://irdb.nii.ac.jp
Original Data Provider (Database): 広島大学 : 広島大学学術情報リポジトリ