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Mitochondrial mislocalization and altered assembly of a cluster of Barth syndrome mutant tafazzins
None of the 28 identified point mutations in tafazzin (Taz1p), which is the mutant gene product associated with Barth syndrome (BTHS), has a biochemical explanation. In this study, endogenous Taz1p was localized to mitochondria in association with both the inner and outer mitochondrial membranes fac...
Tallennettuna:
| Päätekijät: | , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
The Rockefeller University Press
2006
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2064234/ https://ncbi.nlm.nih.gov/pubmed/16880272 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.200605043 |
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