Art
J-GLOBAL ID：200902197031177480   Reference number：97A1026641

Molecular defects in genetic diseases of peroxisomes.

ペルオキシソームの遺伝的疾患における分子的欠損
Author (1)：
FUJIKI Y

About FUJIKI Y

(Kyushu Univ., Fukuoka, JPN)

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Material：
Biochimica et Biophysica Acta  (BBA. Biomembranes)

About Biochimica et Biophysica Acta


Volume： 1361  Issue： 3  Page： 235-250  Publication year： Oct. 24, 1997 
JST Material Number： B0207A  ISSN： 0005-2728  CODEN： BBBMBS  Document type： Article
Article type： 文献レビュー  Country of issue： Netherlands (NLD)  Language： ENGLISH (EN)
Thesaurus term：
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Keywords indexed to the article.
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hereditary disease

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,...
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.
Zellweger syndrome

About Zellweger syndrome


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JST classification (2)：
JST classification
Category name(code) classified by JST.
Congenital diseases,deformities in general. 
(GD03010V)

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,  Molecular genetics in general 
(EC02010J)

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Terms in the title (5)：
Terms in the title
Keywords automatically extracted from the title.
ペルオキシソーム

About ペルオキシソーム

, 
遺伝

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, 
疾患

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, 
分子

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, 
欠損

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