PEX11β Deficiency Is Lethal and Impairs Neuronal Migration but Does Not Abrogate Peroxisome Function

Zellweger syndrome is a lethal neurological disorder characterized by severe defects in peroxisomal protein import. The resulting defects in peroxisome metabolism and the accumulation of peroxisomal substrates are thought to cause the other Zellweger syndrome phenotypes, including neuronal migration...

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Bibliografski detalji
Glavni autori: Li, Xiaoling, Baumgart, Eveline, Morrell, James C., Jimenez-Sanchez, Gerardo, Valle, David, Gould, Stephen J.
Format: Artigo
Jezik:Inglês
Izdano: American Society for Microbiology 2002
Teme:
Mammalian Genetic Models with Minimal or Complex Phenotypes
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC133847/
https://ncbi.nlm.nih.gov/pubmed/12024045
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.22.12.4358-4365.2002
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