Structure of NavAb L98R as a basis for the human Nav1.7 Inherited Erythromelalgia L823R mutation
收藏数据链接：
官方服务：
资源简介：
Structure of NavAb L98R as a basis for the human Nav1.7 Inherited Erythromelalgia L823R mutation Descriptor: 1,2-DIMYRISTOYL-SN-GLYCERO-3-PHOSPHOCHOLINE, Ion transport protein Authors: Wisedchaisri, G, Gamal El-Din, T.M, Zheng, N, Catterall, W.A. Deposit date: 2022-06-29 Release date: 2023-10-25 Last modified: 2026-03-04 Method: X-RAY DIFFRACTION (3.3 Å) Cite: Structural basis for severe pain caused by mutations in the voltage sensors of sodium channel NaV1.7. J.Gen.Physiol., 155, 2023
创建时间：
2022-06-29
