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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Mol Genet Metab
Prif Awduron: 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.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2014
Pynciau:
Article
Mynediad Ar-lein: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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