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Targeted Deletion of the PEX2 Peroxisome Assembly Gene in Mice Provides a Model for Zellweger Syndrome, a Human Neuronal Migration Disorder
Phyllis L. Faust and Mary E. HattenVolume:
139
Language:
english
Journal:
The Journal of Cell Biology
DOI:
10.2307/1618441
Date:
December, 1997
File:
PDF, 2.54 MB
english, 1997