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Defective Peroxisome Membrane Synthesis Due To Mutations in Human PEX3 Causes Zellweger Syndrome, Complementation Group G

✍ Scribed by Ania C. Muntau; Peter U. Mayerhofer; Barbara C. Paton; Stefan Kammerer; Adelbert A. Roscher

Book ID: 117853420
Publisher: American Society of Human Genetics
Year: 2000
Tongue: English
Weight: 837 KB
Volume: 67
Category: Article
ISSN: 0002-9297
DOI: 10.1086/303071

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