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APA Citation
Kausthubham, N., Shukla, A., Gupta, N., Bhavani, G. S., Kulshrestha, S., Das Bhowmik, A., Moirangthem, A., Bijarnia‐Mahay, S., Kabra, M., Puri, R. D., Mandal, K., Verma, I. C., Bielas, S. L., Phadke, S. R., Dalal, A., & Girisha, K. M. (2021). a data set of variants derived from 1455 clinical and research exomes is efficient in variant prioritization for early‐onset monogenic disorders in Indians. Human mutation, 42(4), e15–e61. http://access.bl.uk/ark:/81055/vdc_100127493116.0x00001a