Cite
A de novo PAK1 likely pathogenic variant and a de novo terminal 1q microdeletion in a Chinese girl with global developmental delay, severe intellectual disability, and seizures.
MLA
Zhuang, Jianlong, et al. “A de Novo PAK1 Likely Pathogenic Variant and a de Novo Terminal 1q Microdeletion in a Chinese Girl with Global Developmental Delay, Severe Intellectual Disability, and Seizures.” BMC Medical Genomics, vol. 16, no. 1, Jan. 2023, pp. 1–7. EBSCOhost, https://doi.org/10.1186/s12920-023-01433-x.
APA
Zhuang, J., Xie, M., Yao, J., Fu, W., Zeng, S., Jiang, Y., Wang, Y., Xie, Y., Wang, G., & Chen, C. (2023). A de novo PAK1 likely pathogenic variant and a de novo terminal 1q microdeletion in a Chinese girl with global developmental delay, severe intellectual disability, and seizures. BMC Medical Genomics, 16(1), 1–7. https://doi.org/10.1186/s12920-023-01433-x
Chicago
Zhuang, Jianlong, Meihua Xie, Jianfeng Yao, Wanyu Fu, Shuhong Zeng, Yuying Jiang, Yuanbai Wang, Yingjun Xie, Gaoxiong Wang, and Chunnuan Chen. 2023. “A de Novo PAK1 Likely Pathogenic Variant and a de Novo Terminal 1q Microdeletion in a Chinese Girl with Global Developmental Delay, Severe Intellectual Disability, and Seizures.” BMC Medical Genomics 16 (1): 1–7. doi:10.1186/s12920-023-01433-x.