Yang, X., Zhang, Y., Xu, X., Wang, S., Yang, Z., Wu, Y., . . . Wu, X. (2013). Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis. BioMed Central.
Citación estilo ChicagoYang, Xiaoling, Yuehua Zhang, Xiaojing Xu, Shuang Wang, Zhixian Yang, Ye Wu, Xiaoyan Liu, and Xiru Wu. Phenotypes and PRRT2 Mutations in Chinese Families With Benign Familial Infantile Epilepsy and Infantile Convulsions With Paroxysmal Choreoathetosis. BioMed Central, 2013.
Cita MLAYang, Xiaoling, et al. Phenotypes and PRRT2 Mutations in Chinese Families With Benign Familial Infantile Epilepsy and Infantile Convulsions With Paroxysmal Choreoathetosis. BioMed Central, 2013.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.