博士論文

Analysis of the mechanism underlying a mild phenotype of hereditary coproporphyria due to a homozygous missense mutation in the transcription initiation codon of the coproporphyrinogen III oxidase gene

Icons representing 博士論文
The cover of this title could differ from library to library. Link to Help Page

Available in National Diet Library

Find on the publisher's website

国立国会図書館デジタルコレクション

Digital data available

Check on the publisher's website

DOI[info:doi/10.1016/j.jdermsci.2020.06.006]to the data of the same series

Analysis of the mechanism underlying a mild phenotype of hereditary coproporphyria due to a homozygous missense mutation in the transcription initiation codon of the coproporphyrinogen III oxidase gene

Persistent ID (NDL)
info:ndljp/pid/11679366
Material type
博士論文
Author
福井, 智久
Publisher
-
Publication date
2020-09-30
Material Format
Digital
Capacity, size, etc.
-
Name of awarding university/degree
弘前大学,博士（医学）
View All

Notes on use

Note (General)：

type:Thesis掲載誌：Journal of dermatological science,PubMed番号 : 33008663

Search by Bookstore

Search by Bookstore

Read this material in an accessible format.

View materials in accessible formats for people with print disabilities (1Type)

Search by Bookstore

Read in Disability Resources

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
Title
Analysis of the mechanism underlying a mild phenotype of hereditary coproporphyria due to a homozygous missense mutation in the transcription initiation codon of the coproporphyrinogen III oxidase gene
Author/Editor
福井, 智久
Author Heading
福井, 智久
Publication Date
2020-09-30
Publication Date (W3CDTF)
2020-09-30
Alternative Title
コプロポルフィリノーゲンⅢ酸化酵素遺伝子の開始コドンにホモ接合型ミスセンス変異がみられた軽症の遺伝性コプロポルフィリン症の機序分析
Degree grantor/type
弘前大学
Date Granted
2020-09-30
Date Granted (W3CDTF)
2020-09-30