Zhao, F.; Tang, Q.; Xu, J.; Wang, S.; Li, S.; Zou, X.; Cao, Z.
Dehydrocrenatidine Inhibits Voltage-Gated Sodium Channels and Ameliorates Mechanic Allodia in a Rat Model of Neuropathic Pain. Toxins 2019, 11, 229.
https://doi.org/10.3390/toxins11040229
AMA Style
Zhao F, Tang Q, Xu J, Wang S, Li S, Zou X, Cao Z.
Dehydrocrenatidine Inhibits Voltage-Gated Sodium Channels and Ameliorates Mechanic Allodia in a Rat Model of Neuropathic Pain. Toxins. 2019; 11(4):229.
https://doi.org/10.3390/toxins11040229
Chicago/Turabian Style
Zhao, Fang, Qinglian Tang, Jian Xu, Shuangyan Wang, Shaoheng Li, Xiaohan Zou, and Zhengyu Cao.
2019. "Dehydrocrenatidine Inhibits Voltage-Gated Sodium Channels and Ameliorates Mechanic Allodia in a Rat Model of Neuropathic Pain" Toxins 11, no. 4: 229.
https://doi.org/10.3390/toxins11040229
APA Style
Zhao, F., Tang, Q., Xu, J., Wang, S., Li, S., Zou, X., & Cao, Z.
(2019). Dehydrocrenatidine Inhibits Voltage-Gated Sodium Channels and Ameliorates Mechanic Allodia in a Rat Model of Neuropathic Pain. Toxins, 11(4), 229.
https://doi.org/10.3390/toxins11040229