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...

詳細記述

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書誌詳細
出版年:Mol Genet Metab
主要な著者: 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.
フォーマット: Artigo
言語:Inglês
出版事項: 2014
主題:
Article
オンライン･アクセス: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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