Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patients

Notes on use

Search by Bookstore

You can check the details of this material, its authority (keywords that refer to materials on the same subject, author's name, etc.), etc.

Material Type: 博士論文
Title: Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patients
Author/Editor: Atsushi Ishii [著]
Author Heading: 石井, 敦士イシイ, アツシ
Publication, Distribution, etc.: [Atsushi Ishii]
Publication Date: [2013]
Publication Date (W3CDTF): 2013
Extent: 1冊
Alternative Title: 全エクソーム解析により本邦での小児交互性片麻痺の原因となるATP1A3遺伝子変異を同定したゼンエクソームカイセキニヨリホンポウデノショウニコウゴセイヘンマヒノゲンイントナル ATP1A3 イデンシヘンイオドウテイシタ
Degree grantor/type: 福岡大学
Date Granted: 平成25年3月26日
Date Granted (W3CDTF): 2013
Dissertation Number: 甲第1443号
Degree Type: 博士(医学)
Note (Dissertation): 博士論文
Place of Publication (Country Code): JP
Text Language Code: eng
NDLC: UT51
Target Audience: 一般
Note (General): 博士論文
Holding library: 国立国会図書館
Call No.: UT51-2015-C118
Data Provider (Database): 国立国会図書館 : 国立国会図書館蔵書
https://ndlsearch.ndl.go.jp
Bibliographic ID (NDL): 027079818
http://id.ndl.go.jp/bib/027079818
Bibliographic Record Category (NDL): 213