博士論文

COX10両アレル変異とPMP22欠失を伴ったLeigh脳症の一家系 : 臨床病理学的特徴と分子遺伝学的解析の検討

Icons representing 博士論文

COX10両アレル変異とPMP22欠失を伴ったLeigh脳症の一家系 : 臨床病理学的特徴と分子遺伝学的解析の検討

Material type
博士論文
Author
黒羽, 泰子
Publisher
-
Publication date
-
Material Format
Digital
Capacity, size, etc.
-
Name of awarding university/degree
新潟大学,博士(医学)
View All

Notes on use

Note (General):

新大院博(医)第974号

Search by Bookstore

Table of Contents

fulltext
  • 本文 fulltext

abstract
  • 要旨 abstract

Holdings of Libraries in Japan

This page shows libraries in Japan other than the National Diet Library that hold the material.

Please contact your local library for information on how to use materials or whether it is possible to request materials from the holding libraries.

other

  • Niigata University Academic Repository

    Digital
    You can check the holdings of institutions and databases with which 学術機関リポジトリデータベース(IRDB)(機関リポジトリ) is linked at the site of 学術機関リポジトリデータベース(IRDB)(機関リポジトリ).

Bibliographic Record

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

Digital

Material Type
博士論文
Author/Editor
黒羽, 泰子
Author Heading
Alternative Title
Clinicopathological and molecular features of a family with Leigh encephalopathy and hereditary neuropathy with liability to pressure palsy due to biallelic COX10 mutations and PMP22 deletion
Degree grantor/type
新潟大学
Date Granted
2021-03-23
Dissertation Number
甲第4820号
Degree Type
博士(医学)
Text Language Code
jpn