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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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Mol Genet Metab |
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| Prif Awduron: | , , , , , , , , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2014
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| Pynciau: | |
| 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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