Cite
HARVARD Citation
Georges, A. et al. (2021). Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia. Cardiovascular research. 117 (4), pp. 1154-1165. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Georges, A. et al. (2021). Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia. Cardiovascular research. 117 (4), pp. 1154-1165. [Online].