亨廷顿病中的寡细胞病理:从机制到治疗方法

Costanza Ferrari Bardile1, Carola I Radulescu2, Mahmoud A Pouladi1

  • 1Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, Djavad Mowafaghian Centre for Brain Health, British Columbia Children's Hospital Research Institute, University of British Columbia, Vancouver, BC V5Z 4H4, Canada.

PubMed
概括

寡细胞功能障碍有助于神经退行性疾病,如亨廷顿病. 突变的亨廷丁蛋白质损害了髓发育,提供了新的治疗点.

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