- Author:
	        		
		        		
		        		
			        		Xiao-Jing FANG
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Wei ZHANG
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		He LYU
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Zhao-Xia WANG
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Wei-Wei WANG
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Yun YUAN
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		
		        		
		        		
		        		
			        		
			        		Author Information
			        		
 - Publication Type:Case Reports
 - MeSH: Child; Female; Hereditary Sensory and Motor Neuropathy; genetics; Heterozygote; Humans; Mitochondrial Proteins; genetics; Mutation; genetics; Optic Atrophy; genetics; Peptide Termination Factors; genetics
 - From: Chinese Medical Journal 2017;130(2):242-244
 - CountryChina
 - Language:English
 
            
