1. Whole genome and exome sequencing identify NDUFV2 mutations as a new cause of progressive cavitating leukoencephalopathy. Issue 4 (2nd April 2021) Authors: Liu, Zhimei; Zhang, Li; Ren, Changhong; Xu, Manting; Li, Shufang; Ban, Rui; Wu, Ye; Chen, Ling; Sun, Suzhen; Elstner, Matthias; Shimura, Masaru; Ogawa-Tominaga, Minako; Murayama, Kei; Shi, Tieliu; Prokisch, Holger; Fang, Fang Journal: Journal of medical genetics Issue: Volume 59:Issue 4(2022) Page Start: 351 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗