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APA Citation
Bronstein, R., Capowski, E. E., Mehrotra, S., Jansen, A. D., Navarro-Gomez, D., Maher, M., Place, E., Sangermano, R., Bujakowska, K. M., Gamm, D. M., & Pierce, E. A. (2020). a combined RNA-seq and whole genome sequencing approach for identification of non-coding pathogenic variants in single families. Human molecular genetics, 29, 967–979. http://access.bl.uk/ark:/81055/vdc_100116597243.0x000024