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The Lysosomal Sialic Acid Transporter Sialin Is Required for Normal CNS Myelination
Salla disease and infantile sialic acid storage disease are autosomal recessive lysosomal storage disorders caused by mutations in the gene encoding sialin, a membrane protein that transports free sialic acid out of the lysosome after it is cleaved from sialoglycoconjugates undergoing degradation. A...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Society for Neuroscience
2009
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2820501/ https://ncbi.nlm.nih.gov/pubmed/20007460 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.3005-09.2009 |
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