日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Biallelic Truncating Variants in SCN3B Encoding Nav Channel Subunit β3 Lead to Neurodevelopmental Phenotype with and without Epilepsy and Ataxia

编码Nav通道亚基β3的SCN3B基因双等位基因截断变异会导致神经发育表型,伴或不伴癫痫和共济失调。

Routledge, Nathan; Lammens, Maxime; Maroofian, Reza; Beland, Bakht; Murphy, David; Mir, Asif; Ullah, Zia; Alvi, Javeria Reza; Sultan, Tipu; Efthymiou, Stephanie; Bosmans, Frank; Houlden, Henry

Anxiety and dysautonomia symptoms in patients with a Na(V)1.7 mutation and the potential benefits of low-dose short-acting guanfacine.

Na(V)1.7 突变患者的焦虑和自主神经功能障碍症状以及低剂量短效胍法辛的潜在益处

de Cássia Collaço Rita, Lammens Maxime, Blevins Carley, Rodgers Kristen, Gurau Andrei, Yamauchi Suguru, Kim Christine, Forrester Jeannine, Liu Edward, Ha Jinny, Mei Yuping, Boehm Corrine, Wohler Elizabeth, Sobreira Nara, Rowe Peter C, Valle David, Brock Malcolm V, Bosmans Frank

N-Type Inactivation Variances in Honeybee and Asian Giant Hornet Kv Channels

蜜蜂和亚洲大黄蜂Kv通道中N型失活差异

Hussain, Shahid; De Waele, Jolien; Lammens, Maxime; Bosmans, Frank