arrow
W

Wei Wen

ganzhou municipal hospital
H指数:14
被引数:495

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Genetic analysis of a family with skeletal muscle ion channelopathy and hereditary spastic paraplegia type 7 caused by SCN4A and SPG7 double mutations

携带SCN4A和SPG7双重突变、患有骨骼肌离子通道病及7型遗传性痉挛性截瘫家族的遗传分析

Gene
IF2.4
2025-09-230
PRE
Central role of RIPK1-VDAC1 pathway on cardiac impairment in a non-human primate model of rheumatoid arthritis

RIPK1-VDAC1通路在类风湿关节炎非人灵长类动物模型心脏损害中的核心作用

2018-12-0113
PREAI