Jianmin Liang, Cuijuan Xin, Meiying Xin, Guangliang Wang, & Xuemei Wu. (2023). An insertion mutation of the MECP2 gene in severe neonatal encephalopathy and ocular and oropharyngeal dyskinesia: A case report. BMC.
Chicago Style (17th ed.) CitationJianmin Liang, Cuijuan Xin, Meiying Xin, Guangliang Wang, and Xuemei Wu. An Insertion Mutation of the MECP2 Gene in Severe Neonatal Encephalopathy and Ocular and Oropharyngeal Dyskinesia: A Case Report. BMC, 2023.
MLA (9th ed.) CitationJianmin Liang, et al. An Insertion Mutation of the MECP2 Gene in Severe Neonatal Encephalopathy and Ocular and Oropharyngeal Dyskinesia: A Case Report. BMC, 2023.
Warning: These citations may not always be 100% accurate.