1. BEST1 novel mutation causes Bestrophinopathies in six families with distinct phenotypic diversity. Issue 1 (15th November 2022) Authors: Yang, Shangying; Li, Zhen; Cheng, Wanyu; Ma, Meijiao; Qi, Rui; Rui, Xue; Ren, Yinghua; Sheng, Xunlun; Rong, Weining Journal: Molecular genetics & genomic medicine Issue: Volume 11:Issue 1(2023) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗