中国神经再生研究(英文版) ›› 2017, Vol. 12 ›› Issue (10): 1610-1612.doi: 10.4103/1673-5374.217329

• 观点:脑损伤修复保护与再生 • 上一篇    下一篇

从转换起始因子eIF2B的突变到通过氧化呼吸的故障消失白质疾病

  

  • 收稿日期:2017-10-10 出版日期:2017-10-15 发布日期:2017-10-15

Mitochondrial malfunction in vanishing white matter disease: a disease of the cytosolic translation machinery

Orna Elroy-Stein   

  1. Dept of Cell Research and Immunology, George S. Wise Faculty of Life Sciences; Sagol School of Neuroscience, Tel Aviv University, Israel
  • Received:2017-10-10 Online:2017-10-15 Published:2017-10-15
  • Contact: Orna Elroy-Stein, Ph.D., ornaes@tauex.tau.ac.il.
  • Supported by:

    OES’ work was funded by The Legacy Heritage Bio-Medical Program of the Israel Science Foundation (grant No.1629/13).

摘要:

orcid: 0000-0002-3716-1540 (Orna Elroy-Stein)