Cite
MLA Citation
A. Branchini et al.. “Differential functional readthrough over homozygous nonsense mutations contributes to the bleeding phenotype in coagulation factor VII deficiency.” Journal of thrombosis and haemostasis, vol. 14, n.d., pp. 1994–2000. http://access.bl.uk/ark:/81055/vdc_100038942953.0x000006