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Mahadevan R, Bhoyar RC, Viswanathan N, et al. Genomic analysis of patients in a South Indian Community with autosomal dominant cortical tremor, myoclonus and epilepsy suggests a founder repeat expansion mutation in the . Brain Commun. 2020;3(1):fcaa214doi: 10.1093/braincomms/fcaa214.
Mahadevan, R., Bhoyar, R. C., Viswanathan, N., Rajagopal, R. E., Essaki, B., Suroliya, V., Chelladurai, R., Sankaralingam, S., Shanmugam, G., Vayanakkan, S., Shamim, U., Mathur, A., Jain, A., Imran, M., Faruq, M., Scaria, V., Sivasubbu, S., & Kalyanaraman, S. (2021). Genomic analysis of patients in a South Indian Community with autosomal dominant cortical tremor, myoclonus and epilepsy suggests a founder repeat expansion mutation in the . Brain communications, 3(1), fcaa214. https://doi.org/10.1093/braincomms/fcaa214
Mahadevan, Radha, et al. "Genomic analysis of patients in a South Indian Community with autosomal dominant cortical tremor, myoclonus and epilepsy suggests a founder repeat expansion mutation in the ." Brain communications vol. 3,1 (2021): fcaa214. doi: https://doi.org/10.1093/braincomms/fcaa214
Mahadevan R, Bhoyar RC, Viswanathan N, Rajagopal RE, Essaki B, Suroliya V, Chelladurai R, Sankaralingam S, Shanmugam G, Vayanakkan S, Shamim U, Mathur A, Jain A, Imran M, Faruq M, Scaria V, Sivasubbu S, Kalyanaraman S. Genomic analysis of patients in a South Indian Community with autosomal dominant cortical tremor, myoclonus and epilepsy suggests a founder repeat expansion mutation in the . Brain Commun. 2020 Dec 19;3(1):fcaa214. doi: 10.1093/braincomms/fcaa214. eCollection 2021. PMID: 33501421; PMCID: PMC7811760.
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