Genetic Basis of Peroxisome-Assembly Mutants of Humans, Chinese Hamster Ovary Cells, and Yeast: Identification of a New Complementation Group of Peroxisome-Biogenesis Disorders Apparently Lacking Peroxisomal-Membrane Ghosts-Reference-Cited by-同舟云学术

Genetic Basis of Peroxisome-Assembly Mutants of Humans, Chinese Hamster Ovary Cells, and Yeast: Identification of a New Complementation Group of Peroxisome-Biogenesis Disorders Apparently Lacking Peroxisomal-Membrane Ghosts

Published:1998-12 Issue:6 Volume:63 Page:1898-1906
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Shimozawa Nobuyuki,Suzuki Yasuyuki,Zhang Zhongyi,Imamura Atsushi,Kondo Naomi,Kinoshita Naohiko,Fujiki Yukio,Tsukamoto Toshiro,Osumi Takashi,Imanaka Tsuneo,Orii Tadao,Beemer Frits,Mooijer Petra,Dekker Conny,Wanders Ronald J.A.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference34 articles.

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3. Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions: a study using complementation analysis;Brul;J Clin Invest,1988

4. Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders;Chang;Nat Genet,1997

5. Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders;Dodt;Nat Genet,1995

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