Cerebellar defects in Pdss2 conditional knockout mice during embryonic development and in adulthood
PDSS2 is a gene that encodes one of the two subunits of trans-prenyl diphosphate synthase that is essential for ubiquinone biosynthesis. It is known that mutations in PDSS2 can cause primary ubiquinone deficiency in humans and a similar disease in mice. Cerebellum is the most often affected organ in...
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| Autores principales: | , , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Elsevier
2012-01-01
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| Colección: | Neurobiology of Disease |
| Materias: | |
| Acceso en línea: | http://www.sciencedirect.com/science/article/pii/S0969996111002609 |
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