Search Results - Fuwei Luo

  • Showing 1 - 1 results of 1
Refine Results
  1. 1
    Cover Image

    A novel SLC6A8 mutation associated with intellectual disabilities in a Chinese family exhibiting creatine transporter deficiency: case report by Qin Wang, Jingxin Yang, Yang Liu, Xingping Li, Fuwei Luo, Jiansheng Xie

    Published 2018
    Connect to this object online.
    Book

    Save to List
    Saved in:

Search Tools: