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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
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
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
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