Gene mutation detection of one patient with pyruvate dehydrogenase complex deficiency by using next generation sequencing / 中华实用儿科临床杂志
Chinese Journal of Applied Clinical Pediatrics
; (24): 1575-1577, 2016.
Article
in Chinese
| WPRIM (Western Pacific)
| ID: wpr-502178
Responsible library:
WPRO
Full text:
Available
Database:
WPRIM (Western Pacific)
Type of study:
Diagnostic study
Language:
Chinese
Journal:
Chinese Journal of Applied Clinical Pediatrics
Year:
2016
Document type:
Article