Cite
Exome Sequencing Identifies De Novo DYNC1H1 Mutations Associated With Distal Spinal Muscular Atrophy and Malformations of Cortical Development.
MLA
Chen, Yulin, et al. “Exome Sequencing Identifies De Novo DYNC1H1 Mutations Associated With Distal Spinal Muscular Atrophy and Malformations of Cortical Development.” Journal of Child Neurology, vol. 32, no. 4, Mar. 2017, pp. 379–86. EBSCOhost, https://doi.org/10.1177/0883073816683083.
APA
Chen, Y., Xu, Y., Li, G., Li, N., Yu, T., Yao, R., Wang, X., Shen, Y., & Wang, J. (2017). Exome Sequencing Identifies De Novo DYNC1H1 Mutations Associated With Distal Spinal Muscular Atrophy and Malformations of Cortical Development. Journal of Child Neurology, 32(4), 379–386. https://doi.org/10.1177/0883073816683083
Chicago
Chen, Yulin, Yufei Xu, Guoqiang Li, Niu Li, Tingting Yu, Ru-en Yao, Xiumin Wang, Yiping Shen, and Jian Wang. 2017. “Exome Sequencing Identifies De Novo DYNC1H1 Mutations Associated With Distal Spinal Muscular Atrophy and Malformations of Cortical Development.” Journal of Child Neurology 32 (4): 379–86. doi:10.1177/0883073816683083.