Pex13 Inactivation in the Mouse Disrupts Peroxisome Biogenesis and Leads to a Zellweger Syndrome Phenotype

Zellweger syndrome is the archetypical peroxisome biogenesis disorder and is characterized by defective import of proteins into the peroxisome, leading to peroxisomal metabolic dysfunction and widespread tissue pathology. In humans, mutations in the PEX13 gene, which encodes a peroxisomal membrane p...

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में प्रकाशित:	Mol Cell Biol
मुख्य लेखकों:	Maxwell, Megan, Bjorkman, Jonas, Nguyen, Tam, Sharp, Peter, Finnie, John, Paterson, Carol, Tonks, Ian, Paton, Barbara C., Kay, Graham F., Crane, Denis I.
स्वरूप:	Artigo
भाषा:	Inglês
प्रकाशित:	Taylor & Francis 2003
विषय:	Mammalian Genetic Models with Minimal or Complex Phenotypes
ऑनलाइन पहुंच:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC166343/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12897163/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/MCB.23.16.5947-5957.2003
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