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BMP- and neuropilin 1-mediated motor axon navigation relies on spastin alternative translation
Functional analyses of genes responsible for neurodegenerative disorders have unveiled crucial links between neurodegenerative processes and key developmental signalling pathways. Mutations in SPG4-encoding spastin cause hereditary spastic paraplegia (HSP). Spastin is involved in diverse cellular pr...
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| Udgivet i: | Development |
|---|---|
| Main Authors: | , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
The Company of Biologists Ltd
2018
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6141775/ https://ncbi.nlm.nih.gov/pubmed/30082270 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dev.162701 |
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