The Pex1-G844D Mouse: A Model for Mild Human Zellweger Spectrum Disorder

Zellweger spectrum disorder (ZSD) is a disease continuum that results from inherited defects in PEX genes essential for normal peroxisome assembly. These autosomal recessive disorders impact brain development and also cause postnatal liver, adrenal, and kidney dysfunction, as well as loss of vision...

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Dettagli Bibliografici
Pubblicato in:Mol Genet Metab
Autori principali: Hiebler, Shandi, Masuda, Tomohiro, Hacia, Joseph G., Moser, Ann B., Faust, Phyllis L., Liu, Anita, Chowdhury, Nivedita, Huang, Ning, Lauer, Amanda, Bennett, Jean, Watkins, Paul A., Zack, Donald J., Braverman, Nancy E., Raymond, Gerald V., Steinberg, Steven J.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2014
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4901203/
https://ncbi.nlm.nih.gov/pubmed/24503136
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2014.01.008
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