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APA Citation
Janin, A., Chanavat, V., Rollat‐Farnier, P., Bardel, C., Nguyen, K., Chevalier, P., Eicher, J., Faivre, L., Piard, J., Albert, E., Nony, S., & Millat, G. (2020). whole MYBPC3 NGS sequencing as a molecular strategy to improve the efficiency of molecular diagnosis of patients with hypertrophic cardiomyopathy. Human mutation, 41(2), 465–475. http://access.bl.uk/ark:/81055/vdc_100099417843.0x000029