Familial Hemiplegic Migraine Type 3 (FHM3) With an SCN1A Mutation in a Chinese Family: A Case Report

MLA

Na Shao, et al. “Familial Hemiplegic Migraine Type 3 (FHM3) With an SCN1A Mutation in a Chinese Family: A Case Report.” Frontiers in Neurology, vol. 9, Nov. 2018. EBSCOhost, https://doi.org/10.3389/fneur.2018.00976.

APA

Na Shao, Haining Zhang, Xue Wang, Wuqiong Zhang, Miaomiao Yu, & Hongmei Meng. (2018). Familial Hemiplegic Migraine Type 3 (FHM3) With an SCN1A Mutation in a Chinese Family: A Case Report. Frontiers in Neurology, 9. https://doi.org/10.3389/fneur.2018.00976

Chicago

Na Shao, Haining Zhang, Xue Wang, Wuqiong Zhang, Miaomiao Yu, and Hongmei Meng. 2018. “Familial Hemiplegic Migraine Type 3 (FHM3) With an SCN1A Mutation in a Chinese Family: A Case Report.” Frontiers in Neurology 9 (November). doi:10.3389/fneur.2018.00976.