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Dysregulation of human bestrophin-1 by ceramide-induced dephosphorylation
Best vitelliform macular dystrophy is an inherited autosomal dominant, juvenile onset form of macular degeneration caused by mutations in a chloride ion channel, human bestrophin-1 (hBest1). Mutations in Best1 have also been linked to several other forms of retinopathy. In addition to mutations, hBe...
Tallennettuna:
| Päätekijät: | , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Blackwell Science Inc
2009
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2766645/ https://ncbi.nlm.nih.gov/pubmed/19635817 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2009.176800 |
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