Art
J-GLOBAL ID:200902000096586169   Reference number:92A0508780

Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency.

コルチコステロンメチルオキシダーゼII欠損症を起こすヒトCYP11B2(アルドステロンシンターゼ)遺伝子の突然変異
Author (5):
Material:
Volume: 89  Issue: 11  Page: 4996-5000  Publication year: Jun. 01, 1992 
JST Material Number: D0387A  ISSN: 0027-8424  Document type: Article
Article type: 原著論文  Country of issue: United States (USA)  Language: ENGLISH (EN)
Thesaurus term:
Thesaurus term/Semi thesaurus term
Keywords indexed to the article.
All keywords is available on JDreamIII(charged).
On J-GLOBAL, this item will be available after more than half a year after the record posted. In addtion, medical articles require to login to MyJ-GLOBAL.
,...
Semi thesaurus term:
Thesaurus term/Semi thesaurus term
Keywords indexed to the article.
All keywords is available on JDreamIII(charged).
On J-GLOBAL, this item will be available after more than half a year after the record posted. In addtion, medical articles require to login to MyJ-GLOBAL.
,...
   To see more with JDream III (charged).   {{ this.onShowAbsJLink("http://jdream3.com/lp/jglobal/index.html?docNo=92A0508780&from=J-GLOBAL&jstjournalNo=D0387A") }}
JST classification (2):
JST classification
Category name(code) classified by JST.
Congenital diseases,deformities in general.  ,  Structure and chemistry of genes 

Return to Previous Page