Cite
MLA Citation
Lin Ge et al.. “Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy.” Scientific reports, vol. 8, no. 1, 2018, pp. 1–10. http://access.bl.uk/ark:/81055/vdc_100084768195.0x0000ab