Showing 1 - 1 results of 1 for search 'Shuzhang Wei', query time: 0.01s Refine Results
  1. 1
    Concurrent OPA1 mutation and chromosome 3q deletion leading to Behr syndrome: a case report

    Concurrent OPA1 mutation and chromosome 3q deletion leading to Behr syndrome: a case report by Ting Zeng, Linyan Liao, Yi Guo, Xuxu Liu, Xiaobo Xiong, Yu Zhang, Shi Cen, Honghui Li, Shuzhang Wei

    Published 2020
    Connect to this object online.
    Book
    Save to List
    Saved in:

Search Tools: