Cite
HARVARD Citation
Driver, H. et al. (2022). Genomics4RD: An integrated platform to share Canadian deep‐phenotype and multiomic data for international rare disease gene discovery. Human mutation. 43 (6), pp. 800-811. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Driver, H. et al. (2022). Genomics4RD: An integrated platform to share Canadian deep‐phenotype and multiomic data for international rare disease gene discovery. Human mutation. 43 (6), pp. 800-811. [Online].