A Human Gene Responsible for Zellweger Syndrome That Affects Peroxisome Assembly-Reference-Cited by-同舟云学术

A Human Gene Responsible for Zellweger Syndrome That Affects Peroxisome Assembly

Published:1992-02-28 Issue:5048 Volume:255 Page:1132-1134
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Shimozawa Nobuyuki¹²,Tsukamoto Toshiro²,Suzuki Yasuyuki¹,Orii Tadao¹,Shirayoshi Yasuaki²,Mori Takeshi²,Fujiki Yukio²

Affiliation:

1. Department of Pediatrics, Gifu University School of Medicine, Gifu, Gifu 500, Japan

2. Meiji Institute of Health Science, Odawara, Kanagawa 250, Japan.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference20 articles.

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2. BRUL, S, GENETIC-HETEROGENEITY IN THE CEREBROHEPATORENAL (ZELLWEGER) SYNDROME AND OTHER INHERITED DISORDERS WITH A GENERALIZED IMPAIRMENT OF PEROXISOMAL FUNCTIONS - A STUDY USING COMPLEMENTATION ANALYSIS, JOURNAL OF CLINICAL INVESTIGATION 81: 1710 (1988).

3. CHEN, C, HIGH-EFFICIENCY TRANSFORMATION OF MAMMALIAN-CELLS BY PLASMID DNA, MOLECULAR AND CELLULAR BIOLOGY 7: 2745 (1987).

4. CHIRGWIN, J.M., ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE, BIOCHEMISTRY 18: 5294 (1979).

5. GOLDBERG, D.A., ISOLATION AND PARTIAL CHARACTERIZATION OF THE DROSOPHILA ALCOHOL-DEHYDROGENASE GENE, PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES 77: 5794 (1980).

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