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Dissecting the role of the CRMP2–neurofibromin complex on pain behaviors
Neurofibromatosis type 1 (NF1), a genetic disorder linked to inactivating mutations or a homozygous deletion of the Nf1 gene, is characterized by tumorigenesis, cognitive dysfunction, seizures, migraine, and pain. Omic studies on human NF1 tissues identified an increase in the expression of collapsi...
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| 發表在: | Pain |
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| Main Authors: | , , , , , , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2017
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6359908/ https://ncbi.nlm.nih.gov/pubmed/28767512 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/j.pain.0000000000001026 |
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