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“The CAP-Gly of p150: one domain, two diseases, and a function at the end”
In this issue of Neuron, two manuscripts reveal a novel role for p150 in initiation of retrograde transport at synaptic terminals. Moreover, insights are revealed on how mutations of p150's CAP-Gly domain lead to both Perry Syndrome and HMN7B disease.
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| Hoofdauteurs: | , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2012
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4195236/ https://ncbi.nlm.nih.gov/pubmed/22542174 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuron.2012.04.003 |
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