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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Pubblicato in:Pain
Autori principali: Moutal, Aubin, Wang, Yue, Yang, Xiaofang, Ji, Yingshi, Luo, Shizhen, Dorame, Angie, Bellampalli, Shreya S., Chew, Lindsey A., Cai, Song, Dustrude, Erik T., Keener, James E., Marty, Michael T., Vanderah, Todd W., Khanna, Rajesh
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2017
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Article
Accesso online: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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