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CJCP
2020 22 (5):
482-487
ISSN: 1008-8830 CN: 43-1301/R
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Clinical features and SLC6A8 gene mutations of cerebral creatine deficiency syndrome I: an analysis of two families |
SUN Wei-Hua1, ZHUANG Dan-Yan2, WANG Yao1, XIAO Fei-Fan1, WU Meng-Yuan1, DONG Xin-Ran1, ZHANG Ping1, WANG Hui-Jun1, ZHOU Wen-Hao1,3, WU Bing-Bing1 |
Pediatric Research Institute, Children's Hospital, Fudan University, Shanghai 201102, China |
Received: 2020-02-04 Revised: 2020-03-30 Online: null |
Supporting info
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