A novel compound heterozygous mutation in the COA7 gene responsible for a Chinese patient with spinocerebellar ataxia with axonal neuropathy type 3
Author:
Tang Yuwei,Yu Meng,Zhang Wei,Lv He,Deng Jianwen,Liu Jing,Shi Xin,Liang Wei,Jia Zhirong,Yuan Yun,Wang Zhaoxia,Meng Lingchao
Publisher
Dustri-Verlgag Dr. Karl Feistle
Subject
Neurology (clinical),Neurology,General Medicine,Pathology and Forensic Medicine