Cite
APA Citation
Ge, L., Liu, A., Gao, K., Du, R., Ding, J., Mao, B., Hua, Y., Zhang, X., Tan, D., Yang, H., Fu, X., Fan, Y., Zhang, L., Song, S., Wu, J., Zhang, F., Jiang, Y., Wu, X., & Xiong, H. (2018). deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy. Scientific reports, 8(1), 1–10. http://access.bl.uk/ark:/81055/vdc_100084768195.0x0000ab